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Address: 4400 Silver Avenue SE, Albuquerque, New Mexico 87108, USA
www.richmondproducts.com |
Send Inquiry |
Phone: +1-(505)-275-2406
Products: Occluders, Maddox Rods, Bagolini Lenses (FDA Code:
HPD), Fresnel Prism Bars, Trial Frames, Lanthony Tritan, ...
Richmond Products, Inc. produces screening tests & accessories for ophthalmologists and optometrists. Our product includes aniseikonia, phoropter, chin rest, occluders, prisms, novelty, trial frames,
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Address: 3773 Corporate Parkway, Center Valley, Pennsylvania 18034, USA
www.aesculapusa.com |
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Phone: +1-(800)-258-1946
FDA Registration: 2916714 Year Established: 1977
Annual Revenues: USD 1-5 Million
Employee Count: ~120
Products: Curettes, Drills, Titanium Plating Systems, Suction Tubes, Dural Substitute, Posterior, ...
Aesculap Inc. manufactures surgical instrumentation. Our products include surgical instruments, laparoscopy, endoscopy, neurosurgery, sutrures, surgical quality management, and consulting services. Ou
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Address: No. 1 Dayuan St. , Maan Town ZHEJIANG, Shaoxing 312000, China
www.lifehealthcare.net |
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Phone: +86-(575)-88337788
Quality: ISO 9002: 1994 Certified
Products: Elastic Bandages (FDA Code:
FQM), Adhesive Elastic Bandage Tape, Cohesive Elastic Bandage, Cohesive Elastic Bandage Wrap, Rubber Elastic Bandages, Elastic Bandage with Removable Clip, ...
Shaoxing Life Surgical Dressing Co., Ltd. manufactures products for health care industries. The products are gauze sponges, pads, gauze dressings, bandages, swabs, absorbent cotton wool, adhesive tape
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FDA Code / Regulation: HKD / 886.1905 Nystagmus tape is a device that is a long, narrow strip of fabric or other flexible material on which a series of objects are printed. The device is intended to be moved across a patient's field of vision to elicit optokinetic nystagmus (abnormal and irregular eye movements) and to test for blindness.
Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 886.9. The 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.