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Sechrist Industries, Inc.

FDA UDI

Class II (US FDA UDI)

by Sechrist Industries Inc

Identity

Trade Name
Sechrist Industries, Inc. FDA UDI
Generic Name
Orthopaedic stretcher FDA UDI
Device Name
GURNEY W/STRCH,MATT.STANDARD/BARIATRIC FDA UDI
Model / Reference
21709-03 FDA UDI
Description
GURNEY W/STRCH,MATT.STANDARD/BARIATRIC FDA UDI

Identifiers

Primary DI / UDI-DI
00852682007989 FDA UDI
FDA Product Code
FPO FDA UDI
GMDN Term
Orthopaedic stretcher FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6910 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

Yes

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

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 53 Inch FDA UDI
Height — 63 Inch FDA UDI
Weight — 300 Pound FDA UDI
Depth — 92 Inch FDA UDI

Category: Orthopaedic stretcher

Sechrist Industries, Inc. by Sechrist Industries Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic stretcher.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sechrist Industries Inc

Sources (1)

  • FDA UDI 8d7e2c92-7ffd-4321-822e-6b15d775415a 35 fields · synced Jun 8, 2026