Identity
- Trade Name
- Cirrus Ceiling Lift - Tollos FDA UDI
- Generic Name
- Overhead track patient lifting/transfer system FDA UDI
- Device Name
- 600 lbs Capacity Cloth belt G Series Quick Release Dock charging 4-function hand controller 6-point spreader bar (Fixed) FDA UDI
- Model / Reference
- FC-6-FB-F46-FL-FZ FDA UDI
- Description
- 600 lbs Capacity Cloth belt G Series Quick Release Dock charging 4-function hand controller 6-point spreader bar (Fixed) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817956021085 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
No
FDA UDI
Dimensions & Sizes
- Size
- Height — 8 Inch FDA UDIWidth — 13 Inch FDA UDIDepth — 13 Inch FDA UDI
Category: Overhead track patient lifting/transfer system
Cirrus Ceiling Lift - Tollos by 1073849 Ontario Limited — 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
- M-SERIES — Savaria Concord Lifts Inc · 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
- 1073849 Ontario Limited
Sources (1)
- FDA UDI 56f62299-3edd-4683-acea-2e5dc5d4d478 34 fields · synced May 30, 2026