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Hollister

by Hollister Incorporated 564 variants

Ref 9632

Hollister (9632) is a Class I device made by Hollister Incorporated, registered in EUDAMED on 25 Apr 2025 (Basic UDI-DI 610075D03P016S0267AF), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number610075D03P016S0267AF Basic UDI-DI Date25 Apr 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Urinary Leg Bag Plus Connector
Model / reference
9632
Primary DI / UDI-DI
00610075056873, 00610075029785
Basic UDI-DI
610075D03P016S0267AF
Unit of use DI
00610075090099
EMDN code
A06030301 Urine collection bags
Device class
Class I
EU registration type
Standard device
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
US-MF-000027818
Authorised representative
Hollister ULC IE-AR-000022119

Similar devices in this category

Other devices filed under URINE COLLECTION BAGS.

Other devices from Hollister Incorporated

See all devices from Hollister Incorporated →

Properties

  • Supplied sterile
Other properties (13, all answered No)