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M1

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
M1 FDA UDI
Generic Name
Ambulance stretcher, manual FDA UDI
Model / Reference
6100 FDA UDI

Identifiers

Catalog Number
6100-003-000 FDA UDI
Primary DI / UDI-DI
07613327261530 FDA UDI
FDA Product Code
FPO FDA UDI
GMDN Term
Ambulance stretcher, manual 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

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: Ambulance stretcher, manual

M1 by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ambulance stretcher, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 2e93fbee-479f-41ff-9f52-90b8524cdc36 33 fields · synced May 31, 2026