Identity
- Trade Name
- Salvafix Memory PRO FDA UDI
- Generic Name
- Limb/torso/head restraint, reusable FDA UDI
- Device Name
- Restraint ankle band with velcro size S FDA UDI
- Model / Reference
- SVF3351 FDA UDI
- Description
- Restraint ankle band with velcro size S FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08436035356003 FDA UDI
- FDA Product Code
- FMQ FDA UDI
- GMDN Term
- Limb/torso/head restraint, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6760 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
MR Unsafe FDA UDI
Category: Limb/torso/head restraint, reusable
Salvafix Memory PRO by Medi Care System Slu — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Limb/torso/head restraint, reusable.
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- MORRISON MEDICAL — MORRISON MEDICAL, 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
- Medi Care System Slu
Sources (1)
- FDA UDI bd3525ae-e80a-4492-86c3-31ad54fc20f9 34 fields · synced May 31, 2026