SchureMed

FDA UDI

Class I (US FDA UDI)

by Schuerch Corporation

Identity

Trade Name: SchureMed FDA UDI
Generic Name: General examination/treatment chair, electric FDA UDI
Device Name: Power Beach Chair (EU) FDA UDI
Model / Reference: 800-0004-EU FDA UDI
Description: Power Beach Chair (EU) FDA UDI

Identifiers

Primary DI / UDI-DI: 00810057373084 FDA UDI
FDA Product Code: GBB FDA UDI
GMDN Term: General examination/treatment chair, electric FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4960 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: General examination/treatment chair, electric

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 6a19e9f3-2398-4dfa-ac41-28b43951e921 34 fields · synced May 31, 2026