← Back to catalogue

Safe Dent

FDA UDI

Class I (US FDA UDI)

by Bgss Company Inc

Identity

Trade Name
SAFE DENT FDA UDI
Generic Name
General-purpose endoscopic needle, single-use FDA UDI
Device Name
A90177BK PRE BENT FLOW TIP 20G BLACK BAG 100 PC FDA UDI
Model / Reference
A90177BK FDA UDI
Description
A90177BK PRE BENT FLOW TIP 20G BLACK BAG 100 PC FDA UDI

Identifiers

Primary DI / UDI-DI
00810339030339 FDA UDI
FDA Product Code
DZM FDA UDI
GMDN Term
General-purpose endoscopic needle, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4730 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: General-purpose endoscopic needle, single-use

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

Similar devices

Also classified as General-purpose endoscopic needle, 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 ba42ee93-ee71-4040-a476-10151311acb5 33 fields · synced May 30, 2026