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Head Sections

FDA UDI

Class II (US FDA UDI)

by Baxter Medical Systems GmbH + Co. KG

Identity

Trade Name
Head Sections FDA UDI
Generic Name
Operating table orthopaedic extension, non-powered FDA UDI
Device Name
Head section double joint V FDA UDI
Model / Reference
1789955 FDA UDI
Description
Head section double joint V FDA UDI

Identifiers

Primary DI / UDI-DI
00887761970885 FDA UDI
FDA Product Code
KXJ FDA UDI
GDC FDA UDI
JEA FDA UDI
GMDN Term
Operating table orthopaedic extension, non-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 FDA UDI
878.4960 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Operating table orthopaedic extension, non-powered

Head Sections by Baxter Medical Systems GmbH + Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating table orthopaedic extension, non-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Baxter Medical Systems GmbH + Co. KG

Sources (1)

  • FDA UDI 5077a18a-dd2b-403e-a523-0cfc141cdfa7 34 fields · synced Jun 8, 2026