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BICEL I/A curved 21G terralution

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref BIT21AModel SMS390S

by Medicel AG

Identity

Trade Name
BICEL I/A curved 21G terralution EUDAMED
BICEL I/A curved / 21G terralution FDA UDI
Generic Name
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use FDA UDI
Device Name
Swiss Coaxial I/A System Soft Tip angled 45° / 21G EUDAMED
I/A handpiece FDA UDI
Model / Reference
SMS390S EUDAMED
BIT21A EUDAMEDFDA UDI
Description
I/A handpiece FDA UDI

Identifiers

Primary DI / UDI-DI
07630055244031 EUDAMEDFDA UDI
Basic UDI-DI
076300552IA03YX EUDAMED
Direct Marketing DI
07630055244031 EUDAMED
FDA Product Code
HMX FDA UDI
EMDN Code
Q021101 OCCULAR IRRIGATION AND ASPIRATION CANNULAS, SINGLE-USE EUDAMED
GMDN Term
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

BICEL I/A curved 21G terralution by Medicel AG — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medicel AG
EUDAMED SRN
CH-MF-000016652
Authorised Representative
Rudolf Riester GmbH DE-AR-000015844

Sources (2)

  • EUDAMED 5dd2d470-5135-4507-b4e6-d88307c3557e 61 fields · synced Jun 19, 2026
  • FDA UDI 149f6037-9ca7-4877-b497-002e6e6fb676 33 fields · synced May 27, 2026