Identity
- Trade Name
- BOOT ALIMED COATED HEEL FDA UDI
- Generic Name
- Foot cushion FDA UDI
- Model / Reference
- 66076 FDA UDI
Identifiers
- Catalog Number
- 2970005919 FDA UDI
- Primary DI / UDI-DI
- 00733657227352 FDA UDI
- FDA Product Code
- FMP FDA UDI
- GMDN Term
- Foot cushion FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6450 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
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Foot cushion
Boot Alimed Coated Heel by AliMed, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Foot cushion.
- PRIMO — Asp Global, LLC · Class I
- HEELIFT GLIDE® Ultra — Walgreen Health Solutions, LLC · Class I
- PRIMO — Asp Global, LLC · Class I
- PRIMO — Asp Global, LLC · Class I
- PRIMO — Asp Global, LLC · Class I
- PRIMO — Asp Global, LLC · Class I
- PRIMO — Asp Global, LLC · Class I
- PRIMO — Asp Global, LLC · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- AliMed, LLC
Sources (1)
- FDA UDI 2c149484-2b20-4967-b2e3-4f18f0c9c4c2 34 fields · synced Jun 9, 2026