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Pads

FDA UDI

Class I (US FDA UDI)

by Baxter Medical Systems GmbH + Co. KG

Identity

Trade Name
Pads FDA UDI
Generic Name
Operating table patient pressure distribution pad, reusable FDA UDI
Device Name
Pad back section U24 FDA UDI
Model / Reference
1551576 FDA UDI
Description
Pad back section U24 FDA UDI

Identifiers

Primary DI / UDI-DI
00887761969957 FDA UDI
FDA Product Code
GDC FDA UDI
KXJ FDA UDI
JEA FDA UDI
GMDN Term
Operating table patient pressure distribution pad, reusable 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

Pads 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 383aaeed-f685-4deb-8749-b991f17aa62d 35 fields · synced May 31, 2026