FDA UDI In Commercial Distribution 🇺🇸 United States

MICOWEY

DI: 06979922960010 · Model: MMABM-1 · Micowey Medical Equipment (Guangxi) Co., LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MICOWEY
Primary DI
06979922960010
Version / Model
MMABM-1
Company Name
Micowey Medical Equipment (Guangxi) Co., LTD
Labeler DUNS
631759374
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-08
Public Version
1
Public Version Date
2026-04-16
Public Version Status
New
Public Device Record Key
9428600c-5104-40b4-a2ae-e1f5e9d7057a

Device Description

Intense Pulsed Light Therapy Device

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

GMDN Terms

Code Name
58935 Intense pulsed light skin surface treatment system

Identifiers

Type ID
Primary 06979922960010

Premarket Submissions

Submission Number Supplement Number
K251545 000