Identity
- Trade Name
- BandGrip® Micro-Anchor® Skin Closure FDA UDI
- Generic Name
- Skin-closure adhesive strip FDA UDI
- Device Name
- 9 cm x 4 cm; w/ 2 Strips, and Perforation FDA UDI
- Model / Reference
- BG1001-F FDA UDI
- Description
- 9 cm x 4 cm; w/ 2 Strips, and Perforation FDA UDI
Identifiers
- Catalog Number
- BG1001-F FDA UDI
- Primary DI / UDI-DI
- 00850010207087 FDA UDI
- FDA Product Code
- GDT FDA UDIFZQ FDA UDIKGX FDA UDIMKY FDA UDI
- GMDN Term
- Skin-closure adhesive strip FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4760 FDA UDI878.4320 FDA UDI880.5240 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Radiation Sterilization FDA UDI
Dimensions & Sizes
- Size
- Width — 4 Centimeter FDA UDILength — 9 Centimeter FDA UDI
BandGrip® Micro-Anchor® Skin Closure by Bandgrip Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Bandgrip Inc.
Sources (1)
- FDA UDI 2970ea2b-a4d1-47ce-a395-6a6816b337f8 37 fields · synced May 31, 2026