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Disposable High Speed Vitrectomy Pack. (20 gauge/ 0.9 mm)

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
Disposable High Speed Vitrectomy Pack. (20 gauge/ 0.9 mm) FDA UDI
Generic Name
Ophthalmic surgical procedure kit, non-medicated, single-use FDA UDI
Model / Reference
4200.US20 FDA UDI

Identifiers

Catalog Number
4200.US20 FDA UDI
Primary DI / UDI-DI
08717872017174 FDA UDI
510(k) Number
K081877 FDA UDI
FDA Product Code
HQC FDA UDI
GMDN Term
Ophthalmic surgical procedure kit, non-medicated, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic surgical procedure kit, non-medicated, single-use

Disposable High Speed Vitrectomy Pack. (20 gauge/ 0.9 mm) by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class II — FDA UDI — listed in…

Similar devices

Also classified as Ophthalmic surgical procedure kit, non-medicated, single-use.

Cleared under the same submission

K081877 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 53ead355-3246-499a-95c9-fa2190920759 34 fields · synced May 30, 2026