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Teat

by Adria Med S.r.l. 14 variants

Ref 02-STA8SGModel TEAT

Teat (02-STA8SG) is a Class IIa device made by Adria Med S.r.l., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 80522047101TTSEPM), 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 Number80522047101TTSEPM Basic UDI-DI 08052204715572UDI-DIDate29 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Teat
Model / reference
TEAT, 02-STA8SG
Primary DI / UDI-DI
08052204715572
Basic UDI-DI
80522047101TTSEPM
EMDN code
V020303 Teats
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.

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Properties

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