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Baby Bottle

by Adria Med S.r.l. 19 variants

Ref 01-255PPModel BABY BOTTLE

Baby Bottle (01-255PP) is a Class IIa device made by Adria Med S.r.l., registered in EUDAMED on 20 Oct 2026 (Basic UDI-DI 80522047101BBSEGV), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number80522047101BBSEGV Basic UDI-DI 08052204715473UDI-DIDate20 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Baby Bottle
Model / reference
BABY BOTTLE, 01-255PP
Primary DI / UDI-DI
08052204715473
Basic UDI-DI
80522047101BBSEGV
EMDN code
V020302 Baby bottles and kit
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000020866

Similar devices in this category

Other devices filed under NEWBORN NUTRITION DEVICES.

Other devices from Adria Med S.r.l.

See all devices from Adria Med S.r.l. →

Properties

  • Supplied sterile
  • Sterilise before use
Other properties (12, all answered No)