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Braval

FDA UDI

Class I (US FDA UDI)

by Patterson Dental Supply, Inc.

Identity

Trade Name
BRAVAL FDA UDI
Generic Name
Non-woven gauze pad, non-sterile FDA UDI
Device Name
Braval® Nonwoven Sponges – 4 Ply 2 X 2 5000 PKG FDA UDI
Model / Reference
070450940 FDA UDI
Description
Braval® Nonwoven Sponges – 4 Ply 2 X 2 5000 PKG FDA UDI

Identifiers

Primary DI / UDI-DI
D6620704509404 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Non-woven gauze pad, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-woven gauze pad, non-sterile

Braval by Patterson Dental Supply, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-woven gauze pad, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e2f1870a-8e0f-41ad-96b6-b572a94a8c5c 33 fields · synced May 30, 2026