Identity
- Trade Name
- UNIVERSAL FOOT BOARD, REFURBISHED FDA UDI
- Generic Name
- Footrest FDA UDI
- Model / Reference
- 6900-51R FDA UDI
Identifiers
- Catalog Number
- 6900-51R FDA UDI
- Primary DI / UDI-DI
- 00842430103711 FDA UDI
- FDA Product Code
- FQO FDA UDI
- GMDN Term
- Footrest FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4960 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: Footrest
Universal Foot Board, Refurbished by Mizuho Orthopedic Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Footrest.
- Ritter — Midmark Corporation · Class I
- Jenx — JENX LIMITED · Class I
- SchureMed — SCHUERCH CORPORATION · Class I
- Ritter — Midmark Corporation · Class I
- Jenx — JENX LIMITED · Class I
- Jenx — JENX LIMITED · Class I
- Jenx — JENX LIMITED · Class I
- Jenx — JENX LIMITED · 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
- Mizuho Orthopedic Systems, Inc.
Sources (1)
- FDA UDI ceb19171-2b7a-47bf-a5d2-e0b1e8a8936b 34 fields · synced Jun 9, 2026