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Matoset Instrument

by Toruńskie Zakłady Materiałów Opatrunkowych Spółka Akcyjna 24 variants

Ref MA-291-DREN-002, MA-291-POJ1-010, MA-291-NAT1-034, MA-291-KLE1-041, MA-291-POJ1-009, MA-291-POJ1-016, MA-291-POJ1-007, MA-291-KLE1-056, MA-291-POJ1-018, MA-291-KLE1-008, MB-291-KLE1-047, MA-291-PENS-008, MA-291-PAT1-009, MA-291-PAT1-015, MA-291-PAT1-003, MA-291-POJ1-021, MA-291-WORM-002, MA-291-POJ1-019, MB-291-POJ1-030, MA-291-KLE1-043, MA-291-NAT1-035, MA-291-NAT1-004, MA-291-WZIE-004, MB-291-POJ1-028, MA-291-POJ1-020, MA-291-PENS-017, MA-291-KONC-002, MA-291-KONC-001, MA-291-KLE1-034, MA-291-PENS-007, MA-291-TROK-002, MA-PR0-7023-002, MB-291-POJ1-023, MA-291-POJ1-028, MA-291-NAT1-012, MA-PR0-7023-001, MB-291-PAT1-018, MA-291-NAT1-016, MB-291-POJ1-026, MA-291-PAT1-018, MA-291-PAT1-024, MA-291-KLE1-047, MA-291-PAT1-005, MA-291-WZIE-003, MA-291-PAT1-022, MA-291-PAT1-027, MA-PR0-4483-005, MA-291-KONC-003, MA-291-PENS-019, MA-291-KLE1-003, MA-291-HACZ-004

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 linked in EUDAMED

A group certificate may exist

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 Number5900516BBCXXXXSK Basic UDI-DI Date29 Jan 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Non-Invasive Disposable Instruments
Surgically Invasive Disposable Instruments
Invasive Disposable Instruments
Model / Reference
MA-291-DREN-002, MA-291-POJ1-010, MA-291-NAT1-034, MA-291-KLE1-041, MA-291-POJ1-009, MA-291-POJ1-016, MA-291-POJ1-007, MA-291-KLE1-056, MA-291-POJ1-018, MA-291-KLE1-008, MB-291-KLE1-047, MA-291-PENS-008, MA-291-PAT1-009, MA-291-PAT1-015, MA-291-PAT1-003, MA-291-POJ1-021, MA-291-WORM-002, MA-291-POJ1-019, MB-291-POJ1-030, MA-291-KLE1-043, MA-291-NAT1-035, MA-291-NAT1-004, MA-291-WZIE-004, MB-291-POJ1-028, MA-291-POJ1-020, MA-291-PENS-017, MA-291-KONC-002, MA-291-KONC-001, MA-291-KLE1-034, MA-291-PENS-007, MA-291-TROK-002, MA-PR0-7023-002, MB-291-POJ1-023, MA-291-POJ1-028, MA-291-NAT1-012, MA-PR0-7023-001, MB-291-PAT1-018, MA-291-NAT1-016, MB-291-POJ1-026, MA-291-PAT1-018, MA-291-PAT1-024, MA-291-KLE1-047, MA-291-PAT1-005, MA-291-WZIE-003, MA-291-PAT1-022, MA-291-PAT1-027, MA-PR0-4483-005, MA-291-KONC-003, MA-291-PENS-019, MA-291-KLE1-003, MA-291-HACZ-004
Primary DI / UDI-DI
05900516331757, 05900516852610, 05900516041793, 05900516868277, 05900516852603, 05900516853372, 05900516852214, 05900516297565, 05900516863838, 05900516849597, 05900516297046, 05900516854379, 05900516845735, 05900516863791, 05900516841164, 05900516865580, 05900516330811, 05900516864460, 05900516867812, 05900516872243, 05900516106911, 05900516848934, 05900516331740, 05900516866570, 05900516865382, 05900516863005, 05900516036782, 05900516028428, 05900516864651, 05900516850081, 05900516037635, 05900516275365, 05900516866464, 05900516867454, 05900516850357, 05900516275358, 05900516298876, 05900516858483, 05900516866495, 05900516865467, 05900516868697, 05900516047306, 05900516841966, 05900516331733, 05900516866716, 05900516296834, 05900516023171, 05900516332624, 05900516866259, 05900516848903, 05900516332631
Basic UDI-DI
5900516BBCXXXXSK, 5900516DDAXXXXTR, 5900516BBOXXXXWP
EMDN Code
V9012, V0402, V0199, V901699
Device Class
Class I
Class IIa
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000002200

Related devices

Category: Surgical retractor/retraction system blade, single-use

Similar devices

Also classified as Surgical retractor/retraction system blade, single-use.

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Properties

  • Sterile

Other properties (12)

  • 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