← Back to catalogue

Insufflation Needle

EUDAMED

Class IIa (EU MDR)

Ref IN-120Model IN SeriesRef IN-150

by Lagis Enterprise Co., Ltd.

Identity

Trade Name
Insufflation Needle EUDAMED
Device Name
Insufflation Needle EUDAMED
Model / Reference
IN Series EUDAMED
IN-120 EUDAMED
IN-150 EUDAMED

Identifiers

Primary DI / UDI-DI
04714123020802 EUDAMED
04714123020819 EUDAMED
Basic UDI-DI
471412302IN-01T3 EUDAMED
EMDN Code
K0104 VERESS NEEDLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain EUDAMED
Iceland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

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

Insufflation Needle by Lagis Enterprise Co., Ltd. — Class IIa — 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
TW-MF-000007081
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED e90adb31-869d-4cc7-9bb1-7d9829e1ee80 61 fields · synced Jul 12, 2026
  • EUDAMED 5f535cbf-9298-4bfd-bdbe-f25e2bdc099e 61 fields · synced May 18, 2026