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Cannu-Hold™ Tubing and Cannula Holder

by Neotech Products LLC

Ref N7035-35Model Cannu-Hold™

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

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number081259401N70350MM Basic UDI-DI 10812594013499UDI-DIDate28 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10812594013499 UDI-DI Date4 Aug 2026ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

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

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  • Withdrawn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
Cannu-Hold™ Tubing and Cannula Holder EUDAMED
Cannu-Hold GUDID
Generic Name
Wearable percutaneous catheter/tube holder, single-use
Model / Ref / Catalog
Cannu-Hold™, N7035-35, Small
Primary DI / UDI-DI
10812594013499 EUDAMED
20812594013496 GUDID
Basic UDI-DI
081259401N70350MM
FDA Product Code
JAY
EMDN Code
M0599 Medical plasters - other
GMDN Term
Wearable percutaneous catheter/tube holder, single-use
Device Class
Class I
Regulation Number
868.5280
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
Cannu-Hold™
N7035-35
GUDID
Small
Primary DI / UDI-DIEUDAMED
10812594013499
GUDID
20812594013496

Manufacturer details

EUDAMED SRN
US-MF-000001895
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Neotech Products LLC

See all devices from Neotech Products LLC →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (19)

  • Sterile: No
  • 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
  • Serial Number: No