TREPSAT FACELIFT DISSECTOR

GUDID 07898789390015

TOYO COMERCIO IMPORTACAO E EXPORTACAO DE INSTRUMENTOS CIRURGICOS LTDA

Open-surgery dissector
Primary Device ID07898789390015
NIH Device Record Key92a7d18d-07c2-4db3-9731-29c5d878aeb6
Commercial Distribution Discontinuation2026-03-23
Commercial Distribution StatusNot in Commercial Distribution
Brand NameTREPSAT FACELIFT DISSECTOR
Version Model NumberP
Company DUNS923345514
Company NameTOYO COMERCIO IMPORTACAO E EXPORTACAO DE INSTRUMENTOS CIRURGICOS LTDA
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107898789390015 [Primary]

FDA Product Code

GDIDissector, Surgical, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07898789390015]

Moist Heat or Steam Sterilization;Ethylene Oxide


[07898789390015]

Moist Heat or Steam Sterilization;Ethylene Oxide


[07898789390015]

Moist Heat or Steam Sterilization;Ethylene Oxide


[07898789390015]

Moist Heat or Steam Sterilization;Ethylene Oxide


[07898789390015]

Moist Heat or Steam Sterilization;Ethylene Oxide


[07898789390015]

Moist Heat or Steam Sterilization;Ethylene Oxide


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-03-31
Device Publish Date2026-03-23

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