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EVOS Cabling System 56-71175691

by Pioneer Surgical Technology Inc.

Ref 71175691

EVOS Cabling System 56-71175691 is a Class I device made by Pioneer Surgical Technology Inc., registered in EUDAMED on 7 Jun 2026 (Basic UDI-DI 019108305016AC001ZS) and listed in FDA GUDID since 1 Feb 2021 (UDI-DI 00191083004006), active as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number019108305016AC001ZS Basic UDI-DI 00191083004006UDI-DIDate7 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00191083004006 UDI-DI Date1 Feb 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 019108305016AC001ZS registered 7 Jun 2026 Active
  • FDA GUDID UDI-DI 00191083004006 listed 1 Feb 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00191083004006
  2. Registered EUDAMED 019108305016AC001ZS

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  • Withdrawn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
EVOS Accessories EUDAMED
EVOS Cabling System GUDID
Generic name
Device sterilization/disinfection container, reusable
Device name
EVOS System Accessories
Model / Ref / Catalog
71175691, 56-71175691
Primary DI / UDI-DI
00191083004006
Basic UDI-DI
019108305016AC001ZS
FDA product code
FSM
EMDN code
S010401 Trays, baskets, tubs for sterilisation and their components
GMDN term
Device sterilization/disinfection container, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
71175691
GUDID
56-71175691

Related devices

Category: Device sterilization/disinfection container, reusable

Similar devices in this category

Other devices filed under TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS.

Other devices from Pioneer Surgical Technology Inc.

See all devices from Pioneer Surgical Technology Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)