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Acrylic Tip

by Steris Corporation 3 variants

Ref PK45112Model Acrylic Tip

Acrylic Tip (PK45112) is a Class I device made by Steris Corporation, registered in EUDAMED on 26 Aug 2026 (Basic UDI-DI 0724995HPACRYLCTPBRSHCC) and listed in FDA GUDID since 31 Mar 2021 (UDI-DI 10724995201941), 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 Number0724995HPACRYLCTPBRSHCC Basic UDI-DI 10724995201941UDI-DIDate26 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10724995201941 UDI-DI Date31 Mar 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0724995HPACRYLCTPBRSHCC registered 26 Aug 2026 Active
  • FDA GUDID UDI-DI 10724995201941 listed 31 Mar 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10724995201941
  2. Registered EUDAMED 0724995HPACRYLCTPBRSHCC

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  • Withdrawn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

Generic name
Surgical instrument/endoscope cleaning utensil, reusable
Model / Ref / Catalog
Acrylic Tip, PK45112
Primary DI / UDI-DI
10724995201941
Basic UDI-DI
0724995HPACRYLCTPBRSHCC
Unit of use DI
00724995201944
FDA product code
MNL
EMDN code
V070101 Endoscopes cleaning brushes - for generic use
GMDN term
Surgical instrument/endoscope cleaning utensil, reusable
Device class
Class I
Regulation number
876.1500
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 10 Millimeter
Length — 16 Inch

Related devices

Category: Surgical instrument/endoscope cleaning utensil, reusable

Similar devices in this category

Other devices filed under CLEANING BRUSHES.

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)