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Microscissors: Vertical.(23 gauge / 0.6 mm)

FDA UDI

Class I (US FDA UDI)

by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Identity

Trade Name
Microscissors: Vertical.(23 gauge / 0.6 mm) FDA UDI
Generic Name
Intraocular scissors, probe-like, reusable FDA UDI
Model / Reference
1286.E06 FDA UDI

Identifiers

Catalog Number
1286.E06 FDA UDI
Primary DI / UDI-DI
08717872005089 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Intraocular scissors, probe-like, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Intraocular scissors, probe-like, reusable

Microscissors: Vertical.(23 gauge / 0.6 mm) by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Intraocular scissors, probe-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Sources (1)

  • FDA UDI c2b38b1b-ab63-49c8-a4cd-01b2303c5075 33 fields · synced May 30, 2026