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Vitrector, M3000, 20GA

FDA UDI

Class II (US FDA UDI)

by Medical Technical Products, Inc

Identity

Trade Name
Vitrector, M3000, 20GA FDA UDI
Generic Name
Vitrectomy system micro-cutting unit FDA UDI
Model / Reference
23-9006 FDA UDI

Identifiers

Primary DI / UDI-DI
00850039020186 FDA UDI
FDA Product Code
HQC FDA UDI
GMDN Term
Vitrectomy system micro-cutting unit 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

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

Yes

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: Vitrectomy system micro-cutting unit

Vitrector, M3000, 20GA by Medical Technical Products, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vitrectomy system micro-cutting unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Technical Products, Inc

Sources (1)

  • FDA UDI f16d3409-916e-4ab7-9bb4-d1657c996269 33 fields · synced May 30, 2026