Non-Powered Ophthalmic Instrument Stand Suppliers
Paul Instruments (india) | Address: 12/3, Tamer Lane, Calcutta, West Bengal 700009, India 
Phone: +91-(33)-22410194
FDA Registration: 8040382
Products: Lacrimal Dilators and Cannulas, Gastroenterologic Needle Holder (FDA Code: FHQ), Lacrimal Probes (FDA Code: HNL), Wilder Lacrimal Dilators, Lacrimal Dilators and Probes, Trabeculotomy Probes, ...
Paul Instruments (india) provides ophthalmic instruments. Our products include caliper, trephine, trial frame, lens clip, trial set, scissors, syringe, lens gauge, cannula, spud, spoon, specula, spatu more...
Phone: +91-(33)-22410194
FDA Registration: 8040382
Products: Lacrimal Dilators and Cannulas, Gastroenterologic Needle Holder (FDA Code: FHQ), Lacrimal Probes (FDA Code: HNL), Wilder Lacrimal Dilators, Lacrimal Dilators and Probes, Trabeculotomy Probes, ...
Paul Instruments (india) provides ophthalmic instruments. Our products include caliper, trephine, trial frame, lens clip, trial set, scissors, syringe, lens gauge, cannula, spud, spoon, specula, spatu more...
Imedos Gmbh | Address: Am Nasstal 4, Jena 07751, Germany 
www.imedos.de | Send Inquiry | Phone: +11-(49)-3641639621
Products: Ophthalmic Instrument Stand (FDA Code: HMG), Non-Powered Ophthalmic Instrument Stand (FDA Code: HMG), AC-Powered Ophthalmic Camera (FDA Code: HKI), Ophthalmic Images Storage Device (FDA Code: NFF), Ophthalmic Images Communications Device (FDA Code: NFG), ...
Imedos Gmbh manufactures medical imaging products. Our imaging products include fundus imaging products, static vessel analysis and dynamic vessel analysis products. Our fundus imaging products includ more...
www.imedos.de | Send Inquiry | Phone: +11-(49)-3641639621
Products: Ophthalmic Instrument Stand (FDA Code: HMG), Non-Powered Ophthalmic Instrument Stand (FDA Code: HMG), AC-Powered Ophthalmic Camera (FDA Code: HKI), Ophthalmic Images Storage Device (FDA Code: NFF), Ophthalmic Images Communications Device (FDA Code: NFG), ...
Imedos Gmbh manufactures medical imaging products. Our imaging products include fundus imaging products, static vessel analysis and dynamic vessel analysis products. Our fundus imaging products includ more...
RZ-Medizintechnik Gmbh | Address: Unter Hasslen 20, Tuttlingen 78532, Germany
www.rz-medizintechnik.com | Phone: +49-(7462)-9470-0
FDA Registration: 9680718 Quality: ISO 9001, EN 46001, DIN EN ISO:13485,CE Certified
Products: Forceps (FDA Code: HTD), Probes (FDA Code: HXB), Surgical Marking Pens (FDA Code: HRP), Gastroenterologic Needle Holder (FDA Code: FHQ), Self-Retaining Retractors (FDA Code: FFO), Lacrimal Probes (FDA Code: HNL), ...
RZ-Medizintechnik GmbH offers standard and speciality instruments & accessories for various surgical fields such as arthroscopy, ENT, urology, ophthalmology, & plastic surgery. We offer a complete set more...
www.rz-medizintechnik.com | Phone: +49-(7462)-9470-0
FDA Registration: 9680718 Quality: ISO 9001, EN 46001, DIN EN ISO:13485,CE Certified
Products: Forceps (FDA Code: HTD), Probes (FDA Code: HXB), Surgical Marking Pens (FDA Code: HRP), Gastroenterologic Needle Holder (FDA Code: FHQ), Self-Retaining Retractors (FDA Code: FFO), Lacrimal Probes (FDA Code: HNL), ...
RZ-Medizintechnik GmbH offers standard and speciality instruments & accessories for various surgical fields such as arthroscopy, ENT, urology, ophthalmology, & plastic surgery. We offer a complete set more...
Suzhou Jinsheng Plastic Co., Ltd. | Address: Xinshi Rd.,Xinjia Industrial, Estate, West Shihu Road, Suzhou, Jiangsu 215028, China 
www.js-sj.com | Send Inquiry | Phone: +86-(512)-6561-6868
FDA Registration: 3005245797 Quality: ISO 9001:2000 Certified
Products: Urine Collection Leg Bags (FDA Code: FAQ), Sterile Leg Urine Collection Bag for External Use (FDA Code: FAQ), Urine Leg Bags (FDA Code: FAQ), Bone Clamp (FDA Code: HXD), Ophthalmic Instrument Stand (FDA Code: HMG), Pediatric Urine Collector (FDA Code: KNX), ...
Suzhou Jinsheng Plastic Co., Ltd. deals with medical disposable materials and health care products. Our product line comprises of piston syringe, first aid kit, hemostatic forceps, triangular graduate more...
www.js-sj.com | Send Inquiry | Phone: +86-(512)-6561-6868
FDA Registration: 3005245797 Quality: ISO 9001:2000 Certified
Products: Urine Collection Leg Bags (FDA Code: FAQ), Sterile Leg Urine Collection Bag for External Use (FDA Code: FAQ), Urine Leg Bags (FDA Code: FAQ), Bone Clamp (FDA Code: HXD), Ophthalmic Instrument Stand (FDA Code: HMG), Pediatric Urine Collector (FDA Code: KNX), ...
Suzhou Jinsheng Plastic Co., Ltd. deals with medical disposable materials and health care products. Our product line comprises of piston syringe, first aid kit, hemostatic forceps, triangular graduate more...
Xinhua Surgical Instrument Co. Ltd. | Address: No. 7 Taimei Road, Zibo New And Hi-Tech Development Zone, Zibo 255086, China
www.xinhuasurgical.com | Phone: +86-(0533)-3595351
FDA Registration: 3005440795
Products: Vaginal Retractors (FDA Code: HDL), Forceps (FDA Code: HTD), Saws (FDA Code: HSO), Gastroenterologic Needle Holder (FDA Code: FHQ), Self-Retaining Retractors (FDA Code: FFO), Bone Hooks (FDA Code: KIK), ...
Xinhua Surgical Instrument Company Ltd. manufactures surgical instruments. Our products include dental instruments, veterinary instruments, sterilizers, autoclaves and dressing containers, electric su more...
www.xinhuasurgical.com | Phone: +86-(0533)-3595351
FDA Registration: 3005440795
Products: Vaginal Retractors (FDA Code: HDL), Forceps (FDA Code: HTD), Saws (FDA Code: HSO), Gastroenterologic Needle Holder (FDA Code: FHQ), Self-Retaining Retractors (FDA Code: FFO), Bone Hooks (FDA Code: KIK), ...
Xinhua Surgical Instrument Company Ltd. manufactures surgical instruments. Our products include dental instruments, veterinary instruments, sterilizers, autoclaves and dressing containers, electric su more...
FDA Code / Regulation: HMG / 886.1860
An ophthalmic instrument stand is an AC-powered or nonpowered device intended to store ophthalmic instruments in a readily accessible position.
Classification. Class I (general controls). The AC-powered device and the battery-powered device are exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 886.9. The battery-powered device is also exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.180, with respect to general requirements concerning records, and 820.198, with respect to complaint files.
