← Back to catalogue

Hillrom™

FDA UDI

Class I (US FDA UDI)

by Baxter Medical Systems GmbH + Co. KG

Identity

Trade Name
Hillrom™ FDA UDI
Generic Name
Operating table orthopaedic extension, non-powered FDA UDI
Device Name
Trumpf Medical/Medizin Leg section two parts spreadable M FDA UDI
Model / Reference
2064465 FDA UDI
Description
Trumpf Medical/Medizin Leg section two parts spreadable M FDA UDI

Identifiers

Primary DI / UDI-DI
00887761992306 FDA UDI
FDA Product Code
GDC FDA UDI
JEA FDA UDI
KXJ FDA UDI
GMDN Term
Operating table orthopaedic extension, non-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 FDA UDI
892.1980 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Hillrom™ by Baxter Medical Systems GmbH + Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Sources (1)

  • FDA UDI 37206ee2-cf81-44d5-87df-3f60a7de978d 35 fields · synced May 31, 2026