Identity
- Trade Name
- Peha-Haft 2.5cmx4m P8 C12 FDA UDI
- Generic Name
- Non-adhesive device retention bandage FDA UDI
- Device Name
- Peha-Haft 2.5cmx4m P8 C12 FDA UDI
- Model / Reference
- 932452 Peha-Haft 2.5cmx4m P8 C12 FDA UDI
- Description
- Peha-Haft 2.5cmx4m P8 C12 FDA UDI
Identifiers
- Catalog Number
- 932452 FDA UDI
- Primary DI / UDI-DI
- 04049500030915 FDA UDI
- FDA Product Code
- FQM FDA UDI
- GMDN Term
- Non-adhesive device retention bandage FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5075 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Category: Non-adhesive device retention bandage
Peha-Haft 2.5cmx4m P8 C12 by Paul Hartmann Corp. — 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
- Paul Hartmann Corp.
Sources (1)
- FDA UDI abc194d5-1693-41f5-bdb6-8f7cc62c9bfe 34 fields · synced May 30, 2026