Identity
- Trade Name
- In-Situ Repositioning Sheet Medium FDA UDI
- Generic Name
- Patient lifting system stretcher FDA UDI
- Model / Reference
- M921539-M FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05056387438900 FDA UDI
- FDA Product Code
- INE FDA UDI
- GMDN Term
- Patient lifting system stretcher FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3910 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
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Patient lifting system stretcher
In-Situ Repositioning Sheet Medium by Silvalea Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Patient lifting system stretcher.
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- INSTALLATION, POWER LOADING SYSTEM, CESSNA 680 * PLS — LIFEPORT, 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 |
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Manufacturer
- Manufacturer
- Silvalea Limited
Sources (1)
- FDA UDI 6139182c-88ab-4ace-9755-21c8718e113a 32 fields · synced May 31, 2026