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OB Pack III

by Arabian Medical Products Manufacturing Company (Enayah) 11 variants

Part of a family of 82 devices: see the family page

Ref 88841-NG10

OB Pack III (88841-NG10) is a Class I device made by Arabian Medical Products Manufacturing Company (Enayah), registered in EUDAMED on 10 Apr 2026 (Basic UDI-DI 6281141EN063LA), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6281141EN063LA Basic UDI-DI 62811410355792UDI-DIDate10 Apr 2026RegisteredStatusActive EUDAMED: not on the EU market

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
O.B & GYN Pack and Drapes
Model / reference
88841-NG10
Primary DI / UDI-DI
62811410355792
Basic UDI-DI
6281141EN063LA
Direct marketing DI
62811410355792
EMDN code
T0202 Surgical procedural kits (excluding surgical instrument kits)
Device class
Class I
EU registration type
Standard device

Manufacturer details

EUDAMED SRN
SA-MF-000012228
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS).

Other devices from Arabian Medical Products Manufacturing Company (Enayah)

See all devices from Arabian Medical Products Manufacturing Company (Enayah) →

Properties

  • Supplied sterile
Other properties (13, all answered No)