Identity
- Trade Name
- KMI IMI Group FDA UDI
- Generic Name
- Dermabrasion brush, manual FDA UDI
- Device Name
- Microdermabrasion Machine FDA UDI
- Model / Reference
- 19-2000 FDA UDI
- Description
- Microdermabrasion Machine FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00851314007298 FDA UDI
- FDA Product Code
- GFD FDA UDI
- GMDN Term
- Dermabrasion brush, manual FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Dermabrasion brush, manual
KMI IMI Group by Innovative Med, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Innovative Med, Inc.
Sources (1)
- FDA UDI b950f390-160c-430e-b36f-c56e4689bc07 33 fields · synced Jun 1, 2026