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I/A Quick Tip for use without irrigation sleeve, 2.8mm

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref VE655235Model MD0105.123 I/A Tips Reusable

by Oertli Instrumente AG

Identity

Trade Name
I/A Quick Tip for use without irrigation sleeve, 2.8mm EUDAMED
Oertli® FDA UDI
Generic Name
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable FDA UDI
Device Name
I/A SPITZE/TIP/POINTE 45°; "QUICK-TIP" 0.35MM; ÖFFNUNG/APRTURE/ORIFICE FDA UDI
Model / Reference
MD0105.123 I/A Tips Reusable EUDAMED
VE655235 EUDAMEDFDA UDI
Description
I/A SPITZE/TIP/POINTE 45°; "QUICK-TIP" 0.35MM; ÖFFNUNG/APRTURE/ORIFICE FDA UDI

Identifiers

Primary DI / UDI-DI
07630003901115 EUDAMEDFDA UDI
Basic UDI-DI
76300039MD0105123V7 EUDAMED
Direct Marketing DI
07630003901115 EUDAMED
FDA Product Code
HQC FDA UDI
EMDN Code
Q020699 PHACOEMULSIFICATION DEVICES - OTHER EUDAMED
GMDN Term
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
886.4670 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

I/A Quick Tip for use without irrigation sleeve, 2.8mm by Oertli Instrumente Ag — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CH-MF-000016175
Authorised Representative
Oertli Ophthalmedic Österreich GmbH AT-AR-000003554

Sources (2)

  • EUDAMED cfba7bbf-ed8d-4d57-8ab3-9a846f1537e7 61 fields · synced Jun 18, 2026
  • FDA UDI a666e416-d123-43b2-80b0-2196530dc760 34 fields · synced May 30, 2026