MF SAFECATH Intravascular catheter 18Gx1.25"

GUDID 28800055100313

Medifirst co., ltd.

Peripheral vascular infusion catheter
Primary Device ID28800055100313
NIH Device Record Key68b7e54d-c1e8-4728-b050-97336573a3a4
Commercial Distribution StatusIn Commercial Distribution
Brand NameMF SAFECATH
Version Model NumberSC107
Catalog NumberIntravascular catheter 18Gx1.25"
Company DUNS688303694
Company NameMedifirst co., ltd.
Device Count50
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800055100319 [Unit of Use]
GS118800055100316 [Primary]
GS128800055100313 [Package]
Contains: 18800055100316
Package: Case [200 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-08-18
Device Publish Date2020-08-10

On-Brand Devices [MF SAFECATH]

28800055100467SC110
28800055100450SS201
28800055100443SS202
28800055100436SS203
28800055100429SS204
28800055100412SS205
28800055100405SS206
28800055100399SS207
28800055100382SS208
28800055100375SC101
28800055100368SC102
28800055100351SC103
28800055100344SC104
28800055100337SC105
28800055100320SC106
28800055100313SC107
28800055100306SC108
28800055100290SC109

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