Skip to content

Verify PCC071

by Steris Corporation

Ref PCC071Model VHP Indicator Tape

Verify PCC071 is a device classified as Class I in the EU and Class II in the US made by Steris Corporation, registered in EUDAMED on 29 Jul 2026 (Basic UDI-DI 0724995PCVERFYVHPTAPEYR), cleared under FDA 510(k) K231488 on 7 Aug 2023 (2 earlier submissions) and listed in FDA GUDID since 6 Jan 2020 (UDI-DI 10724995172593), active as of 23 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None, self-declared

Class I: no certifier involved

510(k) K231488

+2 more

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0724995PCVERFYVHPTAPEYR Basic UDI-DI 10724995172593UDI-DIDate29 Jul 2026RegisteredStatusActive
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK231488 Date7 Aug 2023DecidedStatusActive
United StatesGUDID listing GUDID Number10724995172593 UDI-DI Date6 Jan 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 0724995PCVERFYVHPTAPEYR registered 29 Jul 2026 Active
  • FDA 510(k) K231488 decided 7 Aug 2023 Active· +2 more in the status table
  • FDA GUDID UDI-DI 10724995172593 listed 6 Jan 2020 Listed

Certificates

0 certificates · EUDAMED

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

Timeline

5 dated events

  1. Cleared FDA 510(k) K160485
  2. Cleared FDA 510(k) K183293
  3. Listed FDA GUDID 10724995172593
  4. Cleared FDA 510(k) K231488
  5. Registered EUDAMED 0724995PCVERFYVHPTAPEYR

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Verify
Generic name
Chemical/physical sterilization process indicator
Device name
VHP Indicator Tape
Model / Ref / Catalog
PCC071, VHP Indicator Tape
Primary DI / UDI-DI
10724995172593
Basic UDI-DI
0724995PCVERFYVHPTAPEYR
Unit of use DI
00724995172596
510(k) Number
FDA product code
JOJ
EMDN code
Z12011385 Cleaning, disinfection and sterilisation instruments - consumables
GMDN term
Chemical/physical sterilization process indicator
Device class
Class I EUDAMED
Class II GUDID
Regulation number
880.2800
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
Size
Length — 60 Yard

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: Chemical/physical sterilization process indicator

Cleared under the same submission (K231488)

Similar devices in this category

Other devices filed under CLEANING, DISINFECTION AND STERILISATION INSTRUMENTS - CONSUMABLES.

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
  • Expiration date
Other properties (21, all answered No)