← Back to catalogue

SchureMed

FDA UDI

Class I (US FDA UDI)

by Schuerch Corporation

Identity

Trade Name
SchureMed FDA UDI
Generic Name
Stretcher mattress FDA UDI
Device Name
STRETCHER PAD 30" W X 3.5" H X 76" L DELUXE FDA UDI
Model / Reference
508-1279 FDA UDI
Description
STRETCHER PAD 30" W X 3.5" H X 76" L DELUXE FDA UDI

Identifiers

Primary DI / UDI-DI
00810057370793 FDA UDI
FDA Product Code
FWZ FDA UDI
GMDN Term
Stretcher mattress 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: Stretcher mattress

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

Similar devices

Also classified as Stretcher mattress.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 7bdd138c-4dee-4688-8c8a-32e513b0b1bb 34 fields · synced May 30, 2026