Sally Tube - Tollos

FDA UDI

Class I (US FDA UDI)

by 1073849 Ontario Limited

Identity

Trade Name: Sally Tube - Tollos FDA UDI
Generic Name: Patient transfer/turning sheet, single-use FDA UDI
Device Name: Sally Tube - 58" x 48" (145cm x 125cm) - Single Patient Use FDA UDI
Model / Reference: ST-5848S FDA UDI
Description: Sally Tube - 58" x 48" (145cm x 125cm) - Single Patient Use FDA UDI

Identifiers

Primary DI / UDI-DI: 00817956023232 FDA UDI
FDA Product Code: FSA FDA UDI
GMDN Term: Patient transfer/turning sheet, single-use 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Height — 12 Inch FDA UDI
Width — 10 Inch FDA UDI
Depth — 23 Inch FDA UDI

Category: Patient transfer/turning sheet, single-use

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

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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

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Manufacturer

Manufacturer: 1073849 Ontario Limited

Sources (1)

FDA UDI 41728e10-fd0e-4846-b111-beabd313dfee 34 fields · synced Jun 8, 2026