Identity
- Trade Name
- MedSource Blanket FDA UDI
- Generic Name
- Rescue blanket, reusable FDA UDI
- Device Name
- Curaplex Mylar Blanket 52"x84" FDA UDI
- Model / Reference
- 12945 FDA UDI
- Description
- Curaplex Mylar Blanket 52"x84" FDA UDI
Identifiers
- Catalog Number
- Not Applicable FDA UDI
- Primary DI / UDI-DI
- 00840155408463 FDA UDI
- FDA Product Code
- KME FDA UDI
- GMDN Term
- Rescue blanket, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6060 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
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
Category: Rescue blanket, reusable
MedSource Blanket by Medsource International Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- RHINO RESCUE — Wuxi Emsrun Technology Co., Ltd. · 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 |
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Manufacturer
- Manufacturer
- Medsource International Llc
Sources (1)
- FDA UDI 787ae7e8-c54a-4719-b53e-e225a117465e 34 fields · synced May 29, 2026