← Back to catalogue

Biocide G30

FDA UDI

Class II (US FDA UDI)

by Young Dental Manufacturing I, Llc

Identity

Trade Name
Biocide G30 FDA UDI
Generic Name
Glutaraldehyde device sterilant FDA UDI
Device Name
Glutaraldehyde cold sterilant FDA UDI
Model / Reference
BIOG30CS FDA UDI
Description
Glutaraldehyde cold sterilant FDA UDI

Identifiers

Primary DI / UDI-DI
10302730000020 FDA UDI
510(k) Number
K914749 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

No

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: Glutaraldehyde device sterilant

Biocide G30 by Young Dental Manufacturing I, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glutaraldehyde device sterilant.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d490f482-7235-4414-9ded-583800e93240 34 fields · synced Jun 6, 2026