Identity
- Trade Name
- STRAP PAIR 110 FDA UDI
- Generic Name
- Limb/torso/head restraint, reusable FDA UDI
- Device Name
- Operating table accessory FDA UDI
- Model / Reference
- STRAP PAIR 110 FDA UDI
- Description
- Operating table accessory FDA UDI
Identifiers
- Catalog Number
- 100000110 FDA UDI
- Primary DI / UDI-DI
- 06438435001103 FDA UDI
- FDA Product Code
- FWZ FDA UDI
- GMDN Term
- Limb/torso/head restraint, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4950 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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Limb/torso/head restraint, reusable
Strap Pair 110 by Merivaara Oy — 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
- Merivaara Oy
Sources (1)
- FDA UDI 44cbb283-a597-4617-8c90-c1fd663d4ff2 35 fields · synced May 30, 2026