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Netcell 35-900

by Network Medical Products, Ltd.

Ref 35-900Model PVA Instrument Wipe 2.5” x 2.5” x 2mm

Netcell 35-900 is an ear wick (EU MDD Class I; FDA Class I; FDA product code MDM, Instrument, Manual, Surgical, General Use) made by Network Medical Products, Ltd., registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-05060165018857) and listed in FDA GUDID since 6 Aug 2019 (UDI-DI 05060165018857), active as of 7 Nov 2026.

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

CE MDD

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-05060165018857 Basic UDI-DI 05060165018857UDI-DIDate6 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05060165018857 UDI-DI Date6 Aug 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-05060165018857 registered 6 Nov 2026 Active
  • FDA GUDID UDI-DI 05060165018857 listed 6 Aug 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05060165018857
  2. Registered EUDAMED B-05060165018857

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Netcell© EUDAMED
Netcell GUDID
Generic name
Ear wick, non-biodegradable
Device name
PVA & Cellulose (non-patient contacting, sterile)
Model / reference
35-900, PVA Instrument Wipe 2.5” x 2.5” x 2mm
Primary DI / UDI-DI
05060165018857 EUDAMED
05060165010479 GUDID
Basic UDI-DI
B-05060165018857
FDA product code
MDM
EMDN code
V0799 Products for cleaning medical devices not included in other classes - other
GMDN term
Ear wick, non-biodegradable
Device class
Class I
Regulation number
878.4800
EU registration type
Legacy device (under a directive)
EU market of registration
Malta
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
05060165018857
GUDID
05060165010479

The registries describe this device under different primary UDI-DIs (EUDAMED lists 05060165018857; FDA GUDID lists 05060165010479), so their flags are not compared.

Similar devices in this category

Other devices filed under PRODUCTS FOR CLEANING MEDICAL DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER.

Other devices from Network Medical Products, Ltd.

See all devices from Network Medical Products, Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (18, all answered No)