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Patient Plastics - non sterile

by Medline International France SAS 41 variants

Ref BVGP150-EU, 80302-EU, PM1H4A, 80301-EU, 84890-EU, RL1, 48012-EU, RM2, 84891-EU, 9005-EU, 84888PK-EU, 96360-EU, 84892GR-EU, 49721-EU, PM2H4, 48017-EU, 80006-EU, EMB02B, 80988-EU, 48000-EU, PLBWGRTR120, 05015-EU, 9082EU, 48010-EU, 81000-EU, 49477-EU, 05429A-EU, PLBWGRTR120-B, EMB03B, 80005-EU, PLBWGRTR150, 47544-EU, 30395PKA-EU, 81247-EU, 119542-EU, 30395GR-EU, 47966-EU, PM1H4, RM3, PL1H5A, 48005-EU, 50346A-EU, 49293-EU, PM3H4, PLBWGRTR120-R, 9082EU-B

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 Number0888277DC143NSJU Basic UDI-DI Date12 Mar 2026RegisteredStatusActive

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  • Withdrawn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
Patient Plastics - non sterile
Model / Reference
BVGP150-EU, 80302-EU, PM1H4A, 80301-EU, 84890-EU, RL1, 48012-EU, RM2, 84891-EU, 9005-EU, 84888PK-EU, 96360-EU, 84892GR-EU, 49721-EU, PM2H4, 48017-EU, 80006-EU, EMB02B, 80988-EU, 48000-EU, PLBWGRTR120, 05015-EU, 9082EU, 48010-EU, 81000-EU, 49477-EU, 05429A-EU, PLBWGRTR120-B, EMB03B, 80005-EU, PLBWGRTR150, 47544-EU, 30395PKA-EU, 81247-EU, 119542-EU, 30395GR-EU, 47966-EU, PM1H4, RM3, PL1H5A, 48005-EU, 50346A-EU, 49293-EU, PM3H4, PLBWGRTR120-R, 9082EU-B
Primary DI / UDI-DI
50888277600810, 50888277600735, 40888277451606, 40888277600875, 50888277343120, 00888277443542, 50888277343175, 00888277443566, 40888277600929, 50888277600957, 50888277343083, 50888277600964, 50888277343137, 50888277600698, 40888277443502, 50888277343052, 50888277430226, 30888277447503, 40888277438751, 50888277430967, 50888277443363, 50888277600742, 40888277443328, 50888277600759, 40888277443632, 50888277600834, 40888277425881, 50888277443370, 30888277449552, 50888277343069, 50888277443394, 50888277343045, 40888277425874, 50888277600940, 50888277430219, 50888277343038, 50888277600773, 40888277443496, 00888277443573, 40888277451590, 50888277600889, 50888277600896, 50888277600872, 50888277431612, 40888277443526, 50888277443387, 50888277443332, 50888277600926
Basic UDI-DI
0888277DC143NSJU
Unit of Use DI
00888277600815, 00888277600730, 00888277451608, 00888277600877, 00888277343125, 00888277343170, 00888277600921, 00888277600952, 00888277343088, 00888277600969, 00888277343132, 00888277600693, 00888277443504, 00888277343057, 00888277430221, 00888277447502, 00888277438753, 00888277430962, 00888277443368, 00888277600747, 00888277443320, 00888277600754, 00888277443634, 00888277600839, 00888277425883, 00888277443375, 00888277449551, 00888277343064, 00888277443399, 00888277343040, 00888277425876, 00888277600945, 00888277430214, 00888277343033, 00888277600778, 00888277443498, 00888277451592, 00888277600884, 00888277600891, 00888277431617, 00888277443528, 00888277443382, 00888277443337
EMDN Code
V0402, P099002
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000676

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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