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Exel IV Cath 20GX1"

by Exelint International, Co.

Ref 26741

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00020221267419 Basic UDI-DI 00020221267419UDI-DIDate20 Feb 2024RegisteredStatusActive

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.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Trade Name
Exel IV Cath 20GX1"
EXEL Safelet IV Catheter, 20G x 1”
Device Name
IV Catheter
EXEL Safelet IV Catheter
Model / Reference
26741
Primary DI / UDI-DI
00020221267419
Basic UDI-DI
B-00020221267419, 20221IVCAT267ZT
EMDN Code
A018003, C0101010102
Device Class
Class IIa
EU market of registration
Netherlands
Austria

Manufacturer details

EUDAMED SRN
US-MF-000037396
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Exelint International, Co.

See all devices from Exelint International, Co. →

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No