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Oertli®

FDA UDI

Class II (US FDA UDI)

by Oertli-Instrumente AG

Identity

Trade Name
Oertli® FDA UDI
Generic Name
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable FDA UDI
Device Name
ASPIRATION SPITZE/POINTE 45°; "QUICK-TIP"; 0.3MM ÖFFNUNG/APERTURE/ORIFICE FDA UDI
Model / Reference
VE655515 FDA UDI
Description
ASPIRATION SPITZE/POINTE 45°; "QUICK-TIP"; 0.3MM ÖFFNUNG/APERTURE/ORIFICE FDA UDI

Identifiers

Primary DI / UDI-DI
07630003901160 FDA UDI
FDA Product Code
HQC FDA UDI
GMDN Term
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4670 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

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

Oertli® by Oertli-Instrumente AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6732e16f-9543-4fca-ab87-3efacd717f81 34 fields · synced May 31, 2026