Identity
- Trade Name
- Monarch FDA UDI
- Generic Name
- Overhead track patient lifting/transfer system FDA UDI
- Device Name
- Patient lifter FDA UDI
- Model / Reference
- M929101-02 FDA UDI
- Description
- Patient lifter FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10688503101027 FDA UDI
- FDA Product Code
- FSA FDA UDI
- GMDN Term
- Overhead track patient lifting/transfer system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5510 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Overhead track patient lifting/transfer system
Monarch by Savaria Concord Lifts Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Overhead track patient lifting/transfer system.
- Handicare — HANDICARE USA, INC. · Class I
- Handicare — HANDICARE USA, INC. · Class I
- Handicare — HANDICARE USA, INC. · Class I
- Cirrus Ceiling Lift - Tollos — 1073849 Ontario Limited · Class I
- Handicare — HANDICARE USA, INC. · Class I
- Handicare — HANDICARE USA, INC. · Class I
- M-SERIES — Savaria Concord Lift · Class I
- Handicare — HANDICARE USA, 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
- Savaria Concord Lifts Inc
Sources (1)
- FDA UDI 1ae0e2b4-71c4-430e-8ac4-4a5962ae5a76 33 fields · synced Jun 6, 2026