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Synergetics

FDA UDI

Class II (US FDA UDI)

by Synergetics Usa, Inc.

Identity

Trade Name
Synergetics FDA UDI
Generic Name
Vitrectomy system micro-cutting unit FDA UDI
Device Name
27ga VersaVIT 2.0™ Vitrectomy Probe FDA UDI
Model / Reference
70937 FDA UDI
Description
27ga VersaVIT 2.0™ Vitrectomy Probe FDA UDI

Identifiers

Catalog Number
70937 FDA UDI
Primary DI / UDI-DI
20841305110612 FDA UDI
FDA Product Code
HQE FDA UDI
GMDN Term
Vitrectomy system micro-cutting unit 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

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: Vitrectomy system micro-cutting unit

Synergetics by Synergetics Usa, 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
Synergetics Usa, Inc.

Sources (1)

  • FDA UDI d3a00d14-db11-4171-baae-3d95931e51de 35 fields · synced May 30, 2026