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E3386 Vannas Straight Capsulotomy Scissors

EUDAMEDFDA UDI

Class I (EU MDR)

Ref E3386

by Bausch & Lomb GmbH

Identity

Trade Name
E3386 Vannas Straight Capsulotomy Scissors EUDAMED
Vannas Straight Capsulotomy Scissors FDA UDI
Generic Name
Intraocular scissors, conventional-hinge, reusable FDA UDI
Device Name
Reusable devices EUDAMED
Model / Reference
E3386 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
04058935012267 EUDAMEDFDA UDI
Basic UDI-DI
4058935-000000-AC EUDAMED
Direct Marketing DI
04058935012267 EUDAMED
FDA Product Code
HNF FDA UDI
EMDN Code
L01040510 CAPSULOTOMY SCISSORS, REUSABLE EUDAMED
GMDN Term
Intraocular scissors, conventional-hinge, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
886.4350 FDA UDI
Market of Registration
Netherlands 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Intraocular scissors, conventional-hinge, reusable

E3386 Vannas Straight Capsulotomy Scissors by Bausch & Lomb GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraocular scissors, conventional-hinge, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bausch & Lomb GmbH
EUDAMED SRN
DE-MF-000009142

Sources (2)

  • EUDAMED 0c4094b3-ebf6-4af2-ac42-b0f5945e979e 61 fields · synced Jun 18, 2026
  • FDA UDI 9991a9b3-b75b-4412-9c1f-68d5a265734e 32 fields · synced May 29, 2026