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Nasal Rinse Sachets

by Chengdu Lanrun Biotechnology Co., LTD

Ref 1.35gModel 1.35g、1.62g、1.8g、1.86g、2g、2.16g、2.25g、2.3g、2.34g、2.52g、2.7g、3.6g、4.5g、5.4g

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69502052NRS001JH Basic UDI-DI 06950205200016UDI-DIDate31 Dec 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Nasal Rinse Sachets
Model / Reference
1.35g、1.62g、1.8g、1.86g、2g、2.16g、2.25g、2.3g、2.34g、2.52g、2.7g、3.6g、4.5g、5.4g, 1.35g
Primary DI / UDI-DI
06950205200016
Basic UDI-DI
69502052NRS001JH
EMDN Code
Q030199 Nasopharyngeal devices - other
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000051109
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Properties

Other properties (13)

  • Sterile: No
  • 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