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Bacteria filter 767 ST 6723976

by Drägerwerk AG & Co. KGaA

Ref 6723976Model 1080196K19L030

Bacteria filter 767 ST 6723976 is a device classified as Class I in the EU and Class II in the US made by Drägerwerk AG & Co. KGaA, registered in EUDAMED on 27 May 2026 (Basic UDI-DI 0404867511080196K19L030R2) and listed in FDA GUDID since 22 Jun 2022 (UDI-DI 04048675006053), active as of 12 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, GUDID, synced 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0404867511080196K19L030R2 Basic UDI-DI 04048675006053UDI-DIDate27 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04048675006053 UDI-DI Date22 Jun 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0404867511080196K19L030R2 registered 27 May 2026 Active
  • FDA GUDID UDI-DI 04048675006053 listed 22 Jun 2022 Listed

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Timeline

2 dated events

  1. Listed FDA GUDID 04048675006053
  2. Registered EUDAMED 0404867511080196K19L030R2

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  • Withdrawn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
Bakterienfilter 767 ST EUDAMED
Bacteria filter 767 ST GUDID
Generic name
Suction system filter, microbial
Model / reference
6723976, 1080196K19L030
Primary DI / UDI-DI
04048675006053
Basic UDI-DI
0404867511080196K19L030R2
Unit of use DI
04048675449010
FDA product code
GCX
EMDN code
A060399 Fluid collection bags and systems - other
GMDN term
Suction system filter, microbial
Device class
Class I EUDAMED
Class II GUDID
Regulation number
880.6740
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
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: Suction system filter, microbial

Similar devices in this category

Other devices filed under FLUID COLLECTION BAGS AND SYSTEMS - OTHER.

Other devices from Drägerwerk AG & Co. KGaA

See all devices from Drägerwerk AG & Co. KGaA →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (20, all answered No)