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AMSure® Silicone Coated Latex Foley Catheter 1

by Amsino International, Inc. 10 variants

Ref AS41012, AS41014, AS42022, AS41026, AS41028, AS41016, AS43020, AS43024, AS42018, AS41030, AS41024, AS43018, AS42012, AS41018, AS42014, AS43016, AS42028, AS42020, AS40008

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

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 23 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10704411001522 Basic UDI-DI Date26 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10704411001621 UDI-DI Date23 Sep 2016ListedStatusListed 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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

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  • Withdrawn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
AMSure® Silicone Coated Latex Foley Catheter
Generic Name
Indwelling urethral drainage balloon catheter, non-antimicrobial
Model / Ref / Catalog
AS41012, AS41014, AS42022, AS41026, AS41028, AS41016, AS43020, AS43024, AS42018, AS41030, AS41024, AS43018, AS42012, AS41018, AS42014, AS43016, AS42028, AS42020, AS40008, 1
Primary DI / UDI-DI
10704411001621, 10704411001553, 10704411001607, 10704411001768, 10704411001508, 10704411001737, 10704411001539, 10704411001546, 10704411001706, 10704411001591, 10704411001744, 10704411001614, 10704411001676, 10704411001720, 10704411001522, 10704411001669, 10704411001652, 10704411001638, 10704411001584
Basic UDI-DI
B-10704411001522, B-10704411001539, B-10704411001676, B-10704411001591, B-10704411001607, B-10704411001546, B-10704411001744, B-10704411001768, B-10704411001652, B-10704411001614, B-10704411001584, B-10704411001737, B-10704411001621, B-10704411001553, B-10704411001638, B-10704411001720, B-10704411001706, B-10704411001669, B-10704411001508
510(k) Number
FDA Product Code
EZL
EMDN Code
U020201 Ureteral catheters for occlusion
GMDN Term
Indwelling urethral drainage balloon catheter, non-antimicrobial
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
876.5130
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
AS41012
AS41014
AS42022
AS41026
AS41028
AS41016
AS43020
AS43024
AS42018
AS41030
AS41024
AS43018
AS42012
AS41018
AS42014
AS43016
AS42028
AS42020
AS40008
GUDID
1
Device ClassEUDAMED
Class IIa
GUDID
Class II

Related devices

Category: Indwelling urethral drainage balloon catheter, non-antimicrobial

Cleared under the same submission (K082815)

Show all (12)

Other devices from Amsino International, Inc.

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Properties

  • Sterile
  • Single Use
  • Contains Latex
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (16)

  • Implantable: No
  • Reusable: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No