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Hic-Sig-22

EUDAMED

Class I (EU MDR)

Ref HIC-SIG-22Model Biopsy Forceps (Cold)

by Horizons International Corp.

Identity

Model / Reference
Biopsy Forceps (Cold) EUDAMED
HIC-SIG-22 EUDAMED

Identifiers

Primary DI / UDI-DI
07453047403717 EUDAMED
Basic UDI-DI
74530474387113Z EUDAMED
EMDN Code
G0308010101 GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Category: Flexible endoscopic biopsy forceps, single-use

Hic-Sig-22 by Horizons International Corp. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic biopsy forceps, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CR-MF-000033925
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED a2d2c21e-40d3-4665-a964-808fad0ee86f 61 fields · synced Jul 27, 2026