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QL2030PR

by Atrion Medical Products, Inc.

Part of a family of 45 devices: see the family page

Ref 96482

QL2030PR (96482) is a Class I device made by Atrion Medical Products, Inc., registered in EUDAMED on 8 Sep 2026 (Basic UDI-DI 0856877002QLINFCK) with CE/MDR certificate 2975-MED-2625202 valid until 8 Sep 2031, active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

8 Sep 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SZUTEST Konformitätsbewertungsstelle GmbH

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number2975-MED-2625202 Date9 Sep 2026IssuedStatusActive EUDAMED: not on the EU market expires 8 Sep 2031

Official records

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2975-MED-2625202 Active

    Quality assurance EU MDR

    Certifier
    SZUTEST Konformitätsbewertungsstelle GmbH 2975
    Issued
    9 Sep 2026
    Expires
    8 Sep 2031

Timeline

3 dated events

  1. Registered EUDAMED 0856877002QLINFCK
  2. Certificate issued EUDAMED 2975-MED-2625202
  3. Certificate expires EUDAMED 2975-MED-2625202

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
QL Inflation Device
Model / reference
96482
Primary DI / UDI-DI
04046964773099
Basic UDI-DI
0856877002QLINFCK
EMDN code
A020199 Syringes, single-use - other
Device class
Class I
EU registration type
Standard device

Manufacturer details

EUDAMED SRN
US-MF-000001944
Authorised representative
Emergo Europe B.V. NL-AR-000000116

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Properties

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