← Back to catalogue

Back support sling for Ultramove

FDA UDI

Class I (US FDA UDI)

by 1073849 Ontario Limited

Identity

Trade Name
Back support sling for Ultramove FDA UDI
Generic Name
Stand-up mobile patient lifting system sling/harness FDA UDI
Device Name
Back Support Sling FDA UDI
Model / Reference
TQM2200 FDA UDI
Description
Back Support Sling FDA UDI

Identifiers

Primary DI / UDI-DI
00817956026523 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Stand-up mobile patient lifting system sling/harness 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 — 14 Inch FDA UDI
Width — 6 Inch FDA UDI
Depth — 2 Inch FDA UDI

Category: Stand-up mobile patient lifting system sling/harness

Back support sling for Ultramove by 1073849 Ontario Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stand-up mobile patient lifting system sling/harness.

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

Manufacturer
1073849 Ontario Limited

Sources (1)

  • FDA UDI e2975f25-52df-4010-9ddc-a0e1555b1253 34 fields · synced Jun 6, 2026