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Suction Tip

by GRI Medical & Electronic Technology Co., Ltd.

Ref 70-50140-S, 70-50140Model Straight Tip, Vented

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

CE MDR CE MDD

Valid until

Not listed

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

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
European UnionCE/MDR EUDAMED NumberB-16931918180014 Basic UDI-DI Date26 Jun 2022RegisteredStatusActive
European UnionCE/MDD EUDAMED NumberB-16931918180014 Basic UDI-DI Date26 Jun 2022RegisteredStatusActive
United StatesGUDID listing GUDID Number16931918180014 UDI-DI Date24 Apr 2021ListedStatusListed 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.

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
Alleset
Generic Name
Surgical/emergency suction cannula, non-illuminating, single-use
Device Name
Suction Tip
Model / Reference
Straight Tip EUDAMED
Vented EUDAMED
70-50140-S EUDAMED
70-50140 EUDAMED
Model 70-50140-S GUDID
Primary DI / UDI-DI
16931918180014, 16931918113401
Basic UDI-DI
B-16931918180014, 69319181F100KN
FDA Product Code
JOL
EMDN Code
A06010103 Cannulas and tips for aspiration and irrigation, single-use
GMDN Term
Surgical/emergency suction cannula, non-illuminating, single-use
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
880.6740
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilization Method
Ethylene Oxide

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
Straight Tip, Vented
70-50140-S
70-50140
GUDID
Model 70-50140-S
Device ClassEUDAMED
Class IIa
GUDID
Class II
SterileEUDAMED
Yes
No
GUDID
Yes

Manufacturer details

EUDAMED SRN
CN-MF-000004203
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from GRI Medical & Electronic Technology Co., Ltd.

See all devices from GRI Medical & Electronic Technology Co., Ltd. →

Properties

  • Sterile YesEUDAMEDGUDIDNoEUDAMED
  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration 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
  • Serial Number: No
  • Manufacturing Date: No