Identity
- Trade Name
- CHILDRENS TRACTION BOOTS19131 FDA UDI
- Generic Name
- Operating table orthopaedic extension, non-powered FDA UDI
- Device Name
- Operating table accessory FDA UDI
- Model / Reference
- CHILDRENS TRACTION BOOTS19131 FDA UDI
- Description
- Operating table accessory FDA UDI
Identifiers
- Catalog Number
- 100019131 FDA UDI
- Primary DI / UDI-DI
- 06438435191316 FDA UDI
- FDA Product Code
- FWZ FDA UDI
- GMDN Term
- Operating table orthopaedic extension, non-powered 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: Operating table orthopaedic extension, non-powered
Childrens Traction Boots19131 by Merivaara Oy — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Operating table orthopaedic extension, non-powered.
- General Instruments — ALPHATEC SPINE, INC. · Class I
- Foot plate — Maquet, Inc. · Class I
- 55" Imaging Extension, Kit — Composite Manufacturing, Inc. · Class I
- LIF-PTP — ALPHATEC SPINE, INC. · Class I
- Pivot Guardian — Stryker Corp. · Class I
- Adapter clamp for femur countertraction — Maquet, Inc. · Class I
- Illico — ALPHATEC SPINE, INC. · Class I
- Pelvis plaster cast device — Maquet, Inc. · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Merivaara Oy
Sources (1)
- FDA UDI 459832d2-77c8-4d32-bcd2-51f9775690df 35 fields · synced Jun 6, 2026