← Back to catalogue

Supremo Instrumentos

FDA UDI

Class I (US FDA UDI)

by Andre Gregate Braga Instrumentos Ltda

Identity

Trade Name
Supremo Instrumentos FDA UDI
Generic Name
Hand-held dental retractor FDA UDI
Device Name
Afastador Obwegeser com cabo FDA UDI
Model / Reference
S0914C FDA UDI
Description
Afastador Obwegeser com cabo FDA UDI

Identifiers

Primary DI / UDI-DI
07908854001606 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Hand-held dental retractor 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: Hand-held dental retractor

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 Hand-held dental retractor.

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

Sources (1)

  • FDA UDI 60cdfaae-650d-4ba1-848c-cd8745c0aa50 33 fields · synced May 29, 2026