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SchureMed

FDA UDI

Class I (US FDA UDI)

by Schuerch Corporation

Identity

Trade Name
SchureMed FDA UDI
Generic Name
Operating table patient pressure distribution pad, reusable FDA UDI
Device Name
BERCHTOLD OPERON D850, D750 3" DELUXE FDA UDI
Model / Reference
508-0196 FDA UDI
Description
BERCHTOLD OPERON D850, D750 3" DELUXE FDA UDI

Identifiers

Primary DI / UDI-DI
00810014605005 FDA UDI
FDA Product Code
FWZ FDA UDI
GMDN Term
Operating table patient pressure distribution pad, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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

No

FDA UDI

Category: Operating table patient pressure distribution pad, reusable

SchureMed by Schuerch Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating table patient pressure distribution pad, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Schuerch Corporation

Sources (1)

  • FDA UDI 56c947f9-0eae-4ae2-a994-4197608dd89a 34 fields · synced May 29, 2026