Identity
- Trade Name
- STRAP UNIVERSAL 4IN x 72IN 25/PK FDA UDI
- Generic Name
- Limb/torso/head restraint, reusable FDA UDI
- Model / Reference
- 753925 FDA UDI
Identifiers
- Catalog Number
- 2970009998 FDA UDI
- Primary DI / UDI-DI
- 00733657283631 FDA UDI
- FDA Product Code
- CCX FDA UDI
- GMDN Term
- Limb/torso/head restraint, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.6820 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
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Safe FDA UDI
Category: Limb/torso/head restraint, reusable
STRAP UNIVERSAL 4IN x 72IN 25/PK by AliMed, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Limb/torso/head restraint, reusable.
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- Morrison Medical — MORRISON MEDICAL, LTD · Class I
- Restraint strap — Skytron, LLC · Class I
- E.M Adams co, inc. — E.M. Adams · Class I
- 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
- AliMed, LLC
Sources (1)
- FDA UDI f3be3424-e112-4aff-a898-e09d7ee4279d 34 fields · synced Jun 9, 2026