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SchureMed

FDA UDI

Class I (US FDA UDI)

by Schuerch Corporation

Identity

Trade Name
SchureMed FDA UDI
Generic Name
Operating/examination/treatment table headrest, reusable FDA UDI
Device Name
Disposable Richards Slotted Headrest, Extended FDA UDI
Model / Reference
508-1340 FDA UDI
Description
Disposable Richards Slotted Headrest, Extended FDA UDI

Identifiers

Catalog Number
508-1340 FDA UDI
Primary DI / UDI-DI
00810014600222 FDA UDI
FDA Product Code
FWZ FDA UDI
GMDN Term
Operating/examination/treatment table headrest, 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Operating/examination/treatment table headrest, reusable

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

Similar devices

Also classified as Operating/examination/treatment table headrest, 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 686b7ce8-30ee-480c-a5fe-3c4ab373cc9f 34 fields · synced Jun 1, 2026