← Back to catalogue

Safe Dent

FDA UDI

Class II (US FDA UDI)

by Bgss Company Inc

Identity

Trade Name
SAFE DENT FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
STERLIZATION POUCH E (INNER) FDA UDI
Model / Reference
STP-7004-E FDA UDI
Description
STERLIZATION POUCH E (INNER) FDA UDI

Identifiers

Primary DI / UDI-DI
00854014003140 FDA UDI
FDA Product Code
JOJ FDA UDI
GMDN Term
Sterilization packaging, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2800 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Sterilization packaging, single-use

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

Similar devices

Also classified as Sterilization packaging, single-use.

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

Manufacturer
Bgss Company Inc

Sources (1)

  • FDA UDI c2c14690-a4e1-4473-893c-96b5a950e40a 33 fields · synced May 30, 2026