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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 material application tool, reusable FDA UDI
Device Name
Espatula Almore Optical - Optical Almore Spatula FDA UDI
Model / Reference
S2120OP FDA UDI
Description
Espatula Almore Optical - Optical Almore Spatula FDA UDI

Identifiers

Catalog Number
S2120OP FDA UDI
Primary DI / UDI-DI
07908854000449 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Dental material application tool, 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

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 material application tool, reusable

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 material application tool, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Andre Gregate Braga Instrumentos Ltda

Sources (1)

  • FDA UDI 4bab0f3d-8961-4dc3-b1cf-f23798977371 34 fields · synced Jun 1, 2026