← Back to catalogue

Titan - Tollos

FDA UDI

Class I (US FDA UDI)

by 1073849 Ontario Limited

Identity

Trade Name
Titan - Tollos FDA UDI
Generic Name
Mobile patient lifting system, electrically-powered FDA UDI
Device Name
Changed to TX-1000-TC-TH-T01-TM and TX-1000-TC-TH-T01-TN 1000 Lbs capacity Bariatric Medical Lift Hydraulic system Standard legs/casters Bariatric spreader bar Smart controls Internal battery FDA UDI
Model / Reference
FPL1010X FDA UDI
Description
Changed to TX-1000-TC-TH-T01-TM and TX-1000-TC-TH-T01-TN 1000 Lbs capacity Bariatric Medical Lift Hydraulic system Standard legs/casters Bariatric spreader bar Smart controls Internal battery FDA UDI

Identifiers

Primary DI / UDI-DI
00817956026714 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Mobile patient lifting system, electrically-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5510 FDA UDI
Commercial Distribution
Not 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
Weight — 490 Pound FDA UDI
Height — 72 Inch FDA UDI
Width — 42 Inch FDA UDI
Depth — 75 Inch FDA UDI

Titan - Tollos by 1073849 Ontario Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 2ceeebbd-fd2a-4eef-94d6-cea65625d7cb 35 fields · synced Jun 1, 2026