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Z3

FDA UDI

Class II (US FDA UDI)

by Benco Dental Supply Co.

Identity

Trade Name
Z3 FDA UDI
Generic Name
Glutaraldehyde device sterilant FDA UDI
Device Name
Benco Z3 2.5% 28 DAY GLUT FDA UDI
Model / Reference
3321-102 FDA UDI
Description
Benco Z3 2.5% 28 DAY GLUT FDA UDI

Identifiers

Primary DI / UDI-DI
00366975002471 FDA UDI
FDA Product Code
MED FDA UDI
GMDN Term
Glutaraldehyde device sterilant FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6885 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 1 Gallon FDA UDI

Category: Glutaraldehyde device sterilant

Z3 by Benco Dental Supply Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glutaraldehyde device sterilant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 04fb51a7-2264-41e0-a13c-02ac2a60290a 34 fields · synced May 31, 2026