← Back to catalogue

Capsulotomy tip, extended tip

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref VE201730Model MD0105.137 Capsulotomy Tips Reusable

by Oertli Instrumente AG

Identity

Trade Name
Capsulotomy tip, extended tip EUDAMED
Oertli® FDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
Device Name
KAPSULOTOMIE-SPITZE, FIMOSIS; CAPSULOTOMY PLUG-ON-TIP; POINTE CAPSULOTOMIE FDA UDI
Model / Reference
MD0105.137 Capsulotomy Tips Reusable EUDAMED
VE201730 EUDAMEDFDA UDI
Description
KAPSULOTOMIE-SPITZE, FIMOSIS; CAPSULOTOMY PLUG-ON-TIP; POINTE CAPSULOTOMIE FDA UDI

Identifiers

Primary DI / UDI-DI
07630003900514 EUDAMEDFDA UDI
Basic UDI-DI
76300039MD0105137VJ EUDAMED
Direct Marketing DI
07630003900514 EUDAMED
FDA Product Code
HQC FDA UDI
EMDN Code
Q020699 PHACOEMULSIFICATION DEVICES - OTHER EUDAMED
GMDN Term
Open-surgery electrosurgical handpiece/electrode, bipolar, reusable FDA UDI

Classification

Device Class
Class IIb 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

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

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

Capsulotomy tip, extended tip by Oertli Instrumente Ag — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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

Sources (2)

  • EUDAMED 399fc808-bda8-4d2f-a14e-8c6b528d0e56 61 fields · synced Aug 1, 2026
  • FDA UDI 21bda8ed-4331-43dc-9601-0bedaa6c6297 34 fields · synced May 30, 2026