Identity
- Trade Name
- THERAFIRM SINGLES® FDA UDI
- Generic Name
- Compression/pressure sock/stocking, single-use FDA UDI
- Device Name
- Opaque Knee High Singles 12 pk Dispenser 20-30 Sand X-large FDA UDI
- Model / Reference
- T500E0430 FDA UDI
- Description
- Opaque Knee High Singles 12 pk Dispenser 20-30 Sand X-large FDA UDI
Identifiers
- Catalog Number
- DOKHC2030SXL FDA UDI
- Primary DI / UDI-DI
- 00721734050092 FDA UDI
- FDA Product Code
- DWL FDA UDIFQL FDA UDI
- GMDN Term
- Compression/pressure sock/stocking, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5780 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
Category: Compression/pressure sock/stocking, single-use
Therafirm Singles® by Knit-Rite, Inc — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Knit-Rite, Inc
Sources (1)
- FDA UDI 563b3261-a6a4-4783-9ebf-81924c17a914 34 fields · synced May 31, 2026