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VersaVit

FDA UDI

Class II (US FDA UDI)

by Synergetics Usa, Inc.

Identity

Trade Name
VersaVit FDA UDI
Generic Name
Vitrectomy system FDA UDI
Device Name
VersaVIT™ Vitrectomy System FDA UDI
Model / Reference
VERSAVIT FDA UDI
Description
VersaVIT™ Vitrectomy System FDA UDI

Identifiers

Catalog Number
VERSAVIT FDA UDI
Primary DI / UDI-DI
10841305106045 FDA UDI
FDA Product Code
HQE FDA UDI
GMDN Term
Vitrectomy system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4150 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vitrectomy system

VersaVit by Synergetics Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vitrectomy system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synergetics Usa, Inc.

Sources (1)

  • FDA UDI 20e87d2f-0a88-44df-a477-c43c3afb0421 35 fields · synced Jun 6, 2026