Moohan Enterprise Co. Ltd

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Contact: Song Seop
Web: http://www.moohanfa.com
E-Mail:
Address: 71-53, Hawolkok-Dong, Sungbuk-Gu, Seoul 136-130, Korea, Republic Of
Phone: +82-(2)-9426418 | Fax: +82-(2)-9177630 | Map/Directions >>

Profile: Moohan Enterprise Co. Ltd is engaged in the production of skin and beauty care equipments. Our product line comprises of Meso gun, hydrox peel, Omnica I2PL, RF2 sigma6, Dermatron Ionto and danosu aroma. Our Meso gun syringe infusion pump performs a puncture and injects a micro drop and then goes back automatically. Our Omnica I2PL is a skin treatment system to improve various types of dermatological lesion such as pigmentation, pores, flushing, fine wrinkles and hair removal by irradiating visible rays of complicated wavelength of skin. Our Dermatron stimulating deeply sub layer of skin for 28,000 times in a sec kHz vibrating and removes melanin & harm pigment cell and clean the wastes of pore and pilar cyst. We supply Lumin wood lamp that is a skin diazrosis device which reveals skin color changes not visible to the mere eye examination. Our danosu aroma is designed for women with rose oil, the queen of aroma which makes women more feminine and artemisia princes oil which is good for medical cure, antifungal and disinfection and various kinds of Aromas.

FDA Registration Number: 3008606158
US Agent: Aegis Spine Inc.
Phone: +1-(303)-741-4123 E-Mail:

13 Products/Services (Click for related suppliers)

• Blood Tube Mixer (FDA Code: GLE / 862.2050)

General purpose laboratory equipment labeled or promoted for a specific medical use is a device that is intended to prepare or examine specimens from the human body and that is labeled or promoted for a specific medical use.

• Cosmetic Materials

• Fluorescence Wood's Light Test (FDA Code: GMB / 866.2600)

A Wood's fluorescent lamp is a device intended for medical purposes to detect fluorescent materials (e.g., fluorescein pigment produced by certain microorganisms) as an aid in the identification of these microorganisms. The device aids in the diagnosis of disease.

• General Surgical Manual Instrument (FDA Code: MDM / 878.4800)

A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.

• Intense Pulsed Light (IPL) Systems

• Natural Face Masks

• Radiofrequency Equipment

• Safety Scalpel System

• Skin Care & Beauty Treatment

• Skin Care Peels

• Syringe Infusion Pump

• Ultrasonic Skincare System

• Whole Human Serum (FDA Code: DGR / 866.5700)

A whole human plasma or serum immunological test system is a device that consists of reagents used to measure by immunochemical techniques the proteins in plasma or serum. Measurements of proteins in plasma or serum aid in the diagnosis of any disease concerned with abnormal levels of plasma or serum proteins, e.g., agammaglobulinemia, allergies, multiple myeloma, rheumatoid vasculitis, or hereditary angioneurotic edema.