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WideView Vitrectomy Lens: Flat

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
WideView Vitrectomy Lens: Flat FDA UDI
Generic Name
Therapeutic contact lens FDA UDI
Model / Reference
1284.DW FDA UDI

Identifiers

Catalog Number
1284.DW FDA UDI
Primary DI / UDI-DI
08717872004303 FDA UDI
510(k) Number
K033950 FDA UDI
FDA Product Code
HJK FDA UDI
GMDN Term
Therapeutic contact lens FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1385 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

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: Therapeutic contact lens

WideView Vitrectomy Lens: Flat by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Therapeutic contact lens.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 76cfb0d0-33b7-41b5-b934-be674db038c5 34 fields · synced Jun 6, 2026