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Pst300

FDA UDI

Class II (US FDA UDI)

by Baxter Medical Systems GmbH + Co. KG

Identity

Trade Name
PST300 FDA UDI
Generic Name
Universal operating table, electromechanical FDA UDI
Device Name
PST 300L+ FDA UDI
Model / Reference
2082192 FDA UDI
Description
PST 300L+ FDA UDI

Identifiers

Primary DI / UDI-DI
00887761967960 FDA UDI
FDA Product Code
KXJ FDA UDI
GDC FDA UDI
GMDN Term
Universal operating table, electromechanical 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: Universal operating table, electromechanical

Pst300 by Baxter Medical Systems GmbH + Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Universal operating table, electromechanical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 111ed194-a6b8-4730-aad9-5a64a390ef26 34 fields · synced May 30, 2026