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Sensicare PI Evolution

by Medline Industries, LP 4 variants

Ref MSG9555, MSG9570, MSG9580, MSG9590, MSG9575

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

CE MDR

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number00888277603441 UDI-DI Date3 Aug 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number0888277DC41FSTNK Basic UDI-DI Date27 Feb 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.

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  • Withdrawn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
Sensicare PI Evolution EUDAMED
Medline GUDID
Generic Name
Composite-polymer surgical glove, non-powdered
Model / Ref / Catalog
MSG9555, MSG9570, MSG9580, MSG9590, MSG9575
Primary DI / UDI-DI
00888277603441 EUDAMED
00888277603472 EUDAMED
00888277603496 EUDAMED
00888277603519 EUDAMED
00888277603489 EUDAMED
10888277603516 GUDID
10888277603493 GUDID
10888277603486 GUDID
10888277603479 GUDID
10888277603448 GUDID
Basic UDI-DI
0888277DC41FSTNK
FDA Product Code
KGO
EMDN Code
T01010203 Polyisopren surgical gloves
GMDN Term
Composite-polymer surgical glove, non-powdered
Device Class
Class IIa EUDAMED
Class I GUDID
Regulation Number
878.4460
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
00888277603441
00888277603472
00888277603496
00888277603519
00888277603489
GUDID
10888277603516
10888277603493
10888277603486
10888277603479
10888277603448
Device ClassEUDAMED
Class IIa
GUDID
Class I

Manufacturer details

EUDAMED SRN
US-MF-000009717
Authorised representative
Medline International France FR-AR-000001814

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Lot / Batch Number
  • Serial Number YesGUDIDNoGUDID
  • Expiration Date
  • Manufacturing Date YesGUDIDNoGUDID

Other properties (17)

  • 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
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No