← 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
Medical equipment/instrument drape, single-use FDA UDI
Device Name
B2015P PEACH BIBS 13 X 18 3 PLY FDA UDI
Model / Reference
B2015P FDA UDI
Description
B2015P PEACH BIBS 13 X 18 3 PLY FDA UDI

Identifiers

Primary DI / UDI-DI
00810339030582 FDA UDI
FDA Product Code
NRD FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use 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: Medical equipment/instrument drape, 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 Medical equipment/instrument drape, 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 63cd2be6-f4ec-4b4d-91ac-2469332a218d 33 fields · synced May 30, 2026