Supremo Instrumentos

FDA UDI

Class I (US FDA UDI)

by Andre Gregate Braga Instrumentos Ltda

Identity

Trade Name: Supremo Instrumentos FDA UDI
Generic Name: Periosteal elevator, reusable FDA UDI
Device Name: Tunelizador 5 (DLC) - Tunneler 5 DLC FDA UDI
Model / Reference: S2937B FDA UDI
Description: Tunelizador 5 (DLC) - Tunneler 5 DLC FDA UDI

Identifiers

Catalog Number: S2937B FDA UDI
Primary DI / UDI-DI: 07908854000340 FDA UDI
FDA Product Code: DZN FDA UDI
GMDN Term: Periosteal elevator, reusable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Periosteal elevator, reusable

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

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Also classified as Periosteal elevator, reusable.

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HELMUT ZEPF — Helmut Zepf Medizintechnik GmbH · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Andre Gregate Braga Instrumentos Ltda

Sources (1)

FDA UDI 2961615a-f279-49b3-ab84-c1b2cc1f1ec7 34 fields · synced May 30, 2026