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Trumpf Medical

FDA UDI

Class I (US FDA UDI)

by Baxter Medical Systems GmbH + Co. KG

Identity

Trade Name
TRUMPF MEDICAL FDA UDI
Generic Name
Universal operating table, electromechanical FDA UDI
Device Name
OR table top MR Neuro U FDA UDI
Model / Reference
2064888 FDA UDI
Description
OR table top MR Neuro U FDA UDI

Identifiers

Primary DI / UDI-DI
00887761993204 FDA UDI
FDA Product Code
GDC FDA UDI
JEA FDA UDI
KXJ FDA UDI
GMDN Term
Universal operating table, electromechanical 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
MRI Safety
MR Conditional FDA UDI

Trumpf Medical 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

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Manufacturer

Sources (1)

  • FDA UDI da1c68d2-12d2-4b85-9191-a68cb43fefb2 35 fields · synced Jun 1, 2026