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Supremo Instrumentos

FDA UDI

Class I (US FDA UDI)

by Andre Gregate Braga Instrumentos Ltda

Identity

Trade Name
Supremo Instrumentos FDA UDI
Generic Name
Dental rongeur FDA UDI
Device Name
Forceps Especial Baioneta FDA UDI
Model / Reference
S0243 FDA UDI
Description
Forceps Especial Baioneta FDA UDI

Identifiers

Primary DI / UDI-DI
07908854001538 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Dental rongeur FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental rongeur

Supremo Instrumentos by Andre Gregate Braga Instrumentos Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 10148486-c6ce-4307-85d5-3ef91fbfc640 33 fields · synced May 30, 2026