Identity
- Trade Name
- MUELLER PFTAPE SYSTEM FOR PLANTAR FACITIS FDA UDI
- Generic Name
- Skin-cover adhesive strip, non-antimicrobial FDA UDI
- Device Name
- PFTAPE SYSTEM FOR PLANTAR FASCIITIS 7APP FDA UDI
- Model / Reference
- 6337 FDA UDI
- Description
- PFTAPE SYSTEM FOR PLANTAR FASCIITIS 7APP FDA UDI
Identifiers
- Catalog Number
- 6337 FDA UDI
- Primary DI / UDI-DI
- 00074676633701 FDA UDI
- FDA Product Code
- KGX FDA UDI
- GMDN Term
- Skin-cover adhesive strip, non-antimicrobial FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5240 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
Dimensions & Sizes
- Size
- Width — 0.5 Inch FDA UDILength — 10 Yard FDA UDI
Category: Skin-cover adhesive strip, non-antimicrobial
Mueller Pftape System For Plantar Facitis by Mueller Sports Medicine, 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
- Mueller Sports Medicine, Inc.
Sources (1)
- FDA UDI 8c39770c-9d30-4f42-85a8-71e5debcd307 36 fields · synced Jun 9, 2026