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Zinnanti Surgical

FDA UDI

Class II (US FDA UDI)

by Zinnanti Surgical Design Group Inc

Identity

Trade Name
Zinnanti Surgical FDA UDI
Generic Name
Suction/irrigation tubing, single-use FDA UDI
Device Name
Smoke Evac Derm Adapter Kit-Bovie FDA UDI
Model / Reference
14-4051DHB FDA UDI
Description
Smoke Evac Derm Adapter Kit-Bovie FDA UDI

Identifiers

Primary DI / UDI-DI
G373144051DHB0 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Suction/irrigation tubing, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Suction/irrigation tubing, single-use

Zinnanti Surgical by Zinnanti Surgical Design Group Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation tubing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 546fee9a-74c1-460b-a3a6-5efd5c53a3ab 33 fields · synced May 29, 2026