Ts 7500

FDA UDI

Class I (US FDA UDI)

by Baxter Medical Systems GmbH + Co. KG

Identity

Trade Name: TS 7500 FDA UDI
Generic Name: Patient positioning vacuum pad FDA UDI
Device Name: Power Shuttle (H) FDA UDI
Model / Reference: 1774603 FDA UDI
Description: Power Shuttle (H) FDA UDI

Identifiers

Primary DI / UDI-DI: 00887761974319 FDA UDI
FDA Product Code: JEA FDA UDI
KXJ FDA UDI
GDC FDA UDI
GMDN Term: Patient positioning vacuum pad FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4960 FDA UDI
892.1980 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

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Patient positioning vacuum pad

Ts 7500 by Baxter Medical Systems GmbH + Co. KG — 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: Baxter Medical Systems GmbH + Co. KG

Sources (1)

FDA UDI 3681de4d-9f1a-455c-9a1b-e4d7472e8f66 34 fields · synced May 30, 2026