Identity
- Trade Name
- Kwik-Skan® FDA UDI
- Generic Name
- Liquid-crystal patient thermometer, single-use FDA UDI
- Device Name
- Liquid crystal temperature monitor strip (oval), dispenser box FDA UDI
- Model / Reference
- 5130 FDA UDI
- Description
- Liquid crystal temperature monitor strip (oval), dispenser box FDA UDI
Identifiers
- Catalog Number
- 5130 FDA UDI
- Primary DI / UDI-DI
- B23951301 FDA UDI
- FDA Product Code
- KPD FDA UDI
- GMDN Term
- Liquid-crystal patient thermometer, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2200 FDA UDI
- Commercial Distribution
- Not 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Kwik-Skan® by Trademark Medical, L.l.c. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Trademark Medical, L.l.c.
Sources (1)
- FDA UDI 7e113dc7-6067-4031-ab26-722631a8476d 35 fields · synced Jun 8, 2026