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MENTOR Round High Profile Single Use Saline Breast Implant Sizer

by Mentor 14 variants

Ref 351-3190SZDModel MENTOR Saline Breast Implant Sizers

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

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None ongoing

1 closed

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
United StatesGUDID listing GUDID Number10081317029332 UDI-DI Date15 Sep 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number0081317a000033V Basic UDI-DI 10081317029332UDI-DIDate17 Apr 2026RegisteredStatusActive

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

1 recall · FDA

    • Terminated Z-2591-2014 FDA Class II initiated 2 Jul 2014

    The device labeling is stamped with 330cc and the device is actually 380cc device.

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  • Withdrawn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

Generic Name
Invasive breast implant sizer, fixed, single-use
Device Name
MENTOR Saline Breast Implant Sizers
Model / Ref / Catalog
MENTOR Saline Breast Implant Sizers, 351-3190SZD
Primary DI / UDI-DI
10081317029332
Basic UDI-DI
0081317a000033V
510(k) Number
FDA Product Code
MRD
EMDN Code
P0680 Breast implants - accessories
GMDN Term
Invasive breast implant sizer, fixed, single-use
Device Class
Class IIa EUDAMED
U GUDID
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
U

Manufacturer details

EUDAMED SRN
US-MF-000013525
Authorised representative
MENTOR MEDICAL SYSTEMS B.V. NL-AR-000012734

Other devices from Mentor Corp.

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (18)

  • 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
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No