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M1 6100

by Stryker Corp. 2 variants

Ref 6100-031-000Model 08858250000294RY

M1 6100 (6100-031-000) is a device classified as Class I in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 16 Jun 2026 (Basic UDI-DI 08858250000294RY) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 07613327261561), active as of 24 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858250000294RY Basic UDI-DI 07613327261561UDI-DIDate16 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327261561 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000294RY registered 16 Jun 2026 Active
  • FDA GUDID UDI-DI 07613327261561 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327261561
  2. Registered EUDAMED 08858250000294RY

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
M1-Cot Fastener EUDAMED
M1 GUDID
Generic name
Ambulance stretcher, manual
Device name
EMS Cot - Non-Powered
Model / Ref / Catalog
08858250000294RY, 6100-031-000, 6100
Primary DI / UDI-DI
07613327261561
Basic UDI-DI
08858250000294RY
Direct marketing DI
07613327261561
FDA product code
FPO
EMDN code
V08068099 Medical beds - other accessories
GMDN term
Ambulance stretcher, manual
Device class
Class I EUDAMED
Class II GUDID
Regulation number
880.6910
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
08858250000294RY
6100-031-000
GUDID
6100
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Ambulance stretcher, manual

Similar devices in this category

Other devices filed under MEDICAL BEDS - OTHER ACCESSORIES.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Premarket exempt
  • Serial number
Other properties (23, all answered No)