Hillrom™

FDA UDI

Class I (US FDA UDI)

by Baxter Medical Systems GmbH + Co. KG

Identity

Trade Name: Hillrom™ FDA UDI
Generic Name: X-ray film cassette holder FDA UDI
Device Name: X-Ray Top Set PST 300+ L FDA UDI
Model / Reference: 2080975 FDA UDI
Description: X-Ray Top Set PST 300+ L FDA UDI

Identifiers

Primary DI / UDI-DI: 00887761967977 FDA UDI
FDA Product Code: GDC FDA UDI
KXJ FDA UDI
GMDN Term: X-ray film cassette holder 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

Category: X-ray film cassette holder

Hillrom™ 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 f2fecd2d-de5d-4e97-ab91-6324546de439 34 fields · synced May 30, 2026