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Teleport Glide

by OrbusNeich Medical (Shenzhen) Co., Ltd 11 variants

Ref 9218-150-01, 9235-065-11, 9235-150-11, 9218-090-01, 9235-090-01, 9218-135-11, 9218-200-01, 9218-200-11, 9235-200-01, 9235-200-11, 9235-065-01, 9218-180-11

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 22 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number06934955914737 UDI-DI Date20 Jul 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number69349559921ZV Basic UDI-DI Date27 Nov 2025RegisteredStatusActive

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 22 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  • Withdrawn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
Teleport Glide EUDAMED
Teleport Glide Microcatheter GUDID
Generic Name
Vascular microcatheter
Model / Reference
9218-150-01, 9235-065-11, 9235-150-11, 9218-090-01, 9235-090-01, 9218-135-11, 9218-200-01, 9218-200-11, 9235-200-01, 9235-200-11, 9235-065-01, 9218-180-11
Primary DI / UDI-DI
06934955914737, 06934955914874, 06934955914904, 06934955914713, 06934955914775, 06934955914836, 06934955914751, 06934955914867, 06934955914812, 06934955914928, 06934955914768, 06934955914850
Basic UDI-DI
69349559921ZV
Direct Marketing DI
06934955914737
06934955914874
06934955914904
06934955914713
06934955914775
06934955914836
06934955914751
06934955914867
06934955914812
06934955914928
06934955914768
06934955914850
510(k) Number
FDA Product Code
DQY
EMDN Code
C0104020205 Pharmaceutical infusion and administration intravascular catheters and microcatheters
GMDN Term
Vascular microcatheter
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
870.1250
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

Manufacturer details

EUDAMED SRN
CN-MF-000011345
Authorised representative
Quality First International OÜ EE-AR-000004308

Other devices from OrbusNeich Medical (Shenzhen) Co., Ltd

See all devices from OrbusNeich Medical (Shenzhen) Co., Ltd →

Properties

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

Other properties (19)

  • 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