Identity
- Trade Name
- Exchange Select FDA UDI
- Generic Name
- Adhesive bandage FDA UDI
- Device Name
- Waterproof Transparent Dressing, all one size, 2.36 in X 2.75 in (59 mm x 69 mm) FDA UDI
- Model / Reference
- 614299381025 FDA UDI
- Description
- Waterproof Transparent Dressing, all one size, 2.36 in X 2.75 in (59 mm x 69 mm) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00614299381025 FDA UDI
- FDA Product Code
- KGX FDA UDI
- GMDN Term
- Adhesive bandage FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5240 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
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Exchange Select by Aafes — 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
- Aafes
Sources (1)
- FDA UDI 68d6f4df-5a66-4b62-8486-1256826622a7 35 fields · synced Jun 1, 2026