Identity
- Trade Name
- Tortoise™ Turning & positioning system FDA UDI
- Generic Name
- Patient transfer/turning sheet, single-use FDA UDI
- Device Name
- Standard Tortoise FDA UDI
- Model / Reference
- 1400800 FDA UDI
- Description
- Standard Tortoise FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07323190234639 FDA UDI
- FDA Product Code
- FMR FDA UDI
- GMDN Term
- Patient transfer/turning sheet, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6785 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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Patient transfer/turning sheet, single-use
Tortoise™ Turning & positioning system by Mölnlycke Health Care AB — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Mölnlycke Health Care AB
Sources (1)
- FDA UDI 00ac35c7-19fc-4066-9847-87b7761979d6 35 fields · synced May 30, 2026