← Back to catalogue

Intrepid

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 8065752885

by Alcon Laboratories, Inc.

Identity

Trade Name
Intrepid EUDAMED
INTREPID® FDA UDI
Generic Name
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use FDA UDI
Device Name
Intrepid Transformer I/A Handpiece EUDAMED
INTREPID® Transformer IA HP FDA UDI
Model / Reference
8065752885 EUDAMEDFDA UDI
Description
INTREPID® Transformer IA HP FDA UDI

Identifiers

Primary DI / UDI-DI
00380657528851 EUDAMEDFDA UDI
Basic UDI-DI
038065GMN000217H6 EUDAMED
FDA Product Code
HMX FDA UDI
EMDN Code
Z1212020785 PHACO-VITRECTOMY INSTRUMENTS - CONSUMABLES 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
Belgium 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

Yes

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: Phacoemulsification system handpiece tip, single-use

Intrepid by Alcon Laboratories, Inc. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phacoemulsification system handpiece tip, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
US-MF-000016248
Authorised Representative
Alcon Laboratories Belgium BE-AR-000014721

Sources (2)

  • EUDAMED bc180382-2689-4bf4-afe0-fc27f2a18dea 61 fields · synced Jun 8, 2026
  • FDA UDI 706e8139-be4c-4191-a447-0ad7999247b2 34 fields · synced May 30, 2026