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Safe Dent

FDA UDI

Class I (US FDA UDI)

by Bgss Company Inc

Identity

Trade Name
SAFE DENT FDA UDI
Generic Name
Dental dry field kit FDA UDI
Device Name
A9019W SURGICAL ASPIRATOR TIPS 1/8" white (inner bag 25) FDA UDI
Model / Reference
A9019W FDA UDI
Description
A9019W SURGICAL ASPIRATOR TIPS 1/8" white (inner bag 25) FDA UDI

Identifiers

Primary DI / UDI-DI
00810339030254 FDA UDI
FDA Product Code
EHZ FDA UDI
GMDN Term
Dental dry field kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

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: Dental dry field kit

Safe Dent by Bgss Company Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental dry field kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bgss Company Inc

Sources (1)

  • FDA UDI b6e3a524-8e1b-47ee-8625-acfa057b6aa5 33 fields · synced May 30, 2026