SchureMed

FDA UDI

Class I (US FDA UDI)

by Schuerch Corporation

Identity

Trade Name: SchureMed FDA UDI
Generic Name: Arm procedure positioner, reusable FDA UDI
Device Name: CARBON FIBER ENDREST MAJOR PROCEDURE TABLE FDA UDI
Model / Reference: 800-0029 FDA UDI
Description: CARBON FIBER ENDREST MAJOR PROCEDURE TABLE FDA UDI

Identifiers

Primary DI / UDI-DI: 00810014601489 FDA UDI
FDA Product Code: FWZ FDA UDI
GMDN Term: Arm procedure positioner, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Arm procedure positioner, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Schuerch Corporation

Sources (1)

FDA UDI 72babdab-98d5-4f21-8c0f-48d955e83ad0 34 fields · synced Jun 6, 2026