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PVA Wick and Wipe (1mm)

by Network Medical Products Limited 8 variants

Ref M1-400Model PVA and Cellulose Ophthalmic (Non-sterile, Patient Contacting)

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 24 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number506016501T1_02_PVACELLOSA Basic UDI-DI 05056100707023UDI-DIDate16 Jun 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number05056100707023 UDI-DI Date25 Feb 2020ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 24 Oct 2026.

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  • Withdrawn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
Network
Generic Name
Ophthalmic sponge
Device Name
PVA Wick and Wipe (1mm)
Model / Reference
PVA and Cellulose Ophthalmic (Non-sterile, Patient Contacting), M1-400
Primary DI / UDI-DI
05056100707023 EUDAMED
05056100707016 GUDID
Basic UDI-DI
506016501T1_02_PVACELLOSA
510(k) Number
FDA Product Code
HOZ
EMDN Code
Q0299 Ophthalmic devices - other
GMDN Term
Ophthalmic sponge
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
886.4790
EU market of registration
Northern Ireland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
05056100707023
GUDID
05056100707016
Device ClassEUDAMED
Class I
GUDID
Class II
SterileEUDAMED
No
GUDID
Yes

Manufacturer details

EUDAMED SRN
GB-MF-000025518
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Network Medical Products, Ltd.

See all devices from Network Medical Products, Ltd. →

Properties

  • Sterile NoEUDAMEDYesGUDID
  • Single Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (20)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No