← Back to catalogue

Qubix-Polyglactin

EUDAMED

Class III (EU MDR)

Ref QL 2615

by Qubix Medicare Private Limited

Identity

Trade Name
QUBIX-POLYGLACTIN EUDAMED
Device Name
Braided and Coated Polyglactin 910 Suture EUDAMED
Model / Reference
QL 2615 EUDAMED

Identifiers

Primary DI / UDI-DI
08906122171432 EUDAMED
Basic UDI-DI
890612217ABSK7 EUDAMED
EMDN Code
H010101020203 POLYGLYCOLIC WITH LACTIC ACID MULTIFILAMENT WITHOUT NEEDLE EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Slovakia EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Qubix-Polyglactin by Qubix Medicare Private Limited — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
IN-MF-000042759
Authorised Representative
Meddevices Lifesciences B.V. NL-AR-000000594

Sources (1)

  • EUDAMED dfaf6d48-0dbc-4e38-b68d-4efdfc674b0f 61 fields · synced Jun 18, 2026