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Combi - Tollos

FDA UDI

Class I (US FDA UDI)

by 1073849 Ontario Limited

Identity

Trade Name
Combi - Tollos FDA UDI
Generic Name
General-purpose patient lifting system sling/harness FDA UDI
Device Name
Combi Sling - XLarge - Blue Binding - 6 Loop - Poly Material - Single Patient Use FDA UDI
Model / Reference
T015CXX-PSS FDA UDI
Description
Combi Sling - XLarge - Blue Binding - 6 Loop - Poly Material - Single Patient Use FDA UDI

Identifiers

Primary DI / UDI-DI
00817956022082 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
General-purpose 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Height — 21 Inch FDA UDI
Width — 20 Inch FDA UDI
Depth — 19 Inch FDA UDI

Category: General-purpose patient lifting system sling/harness

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

Similar devices

Also classified as General-purpose patient lifting system sling/harness.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
1073849 Ontario Limited

Sources (1)

  • FDA UDI ed6177db-768e-4803-8f7d-059efd4984e1 34 fields · synced Jun 1, 2026