Primary Device ID | 28800055100290 |
NIH Device Record Key | 0bead5d3-01f3-4931-a47c-16aca6fb32a1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MF SAFECATH |
Version Model Number | SC109 |
Catalog Number | Intravascular catheter 16Gx1.16" |
Company DUNS | 688303694 |
Company Name | Medifirst co., ltd. |
Device Count | 50 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08800055100296 [Unit of Use] |
GS1 | 18800055100293 [Primary] |
GS1 | 28800055100290 [Package] Contains: 18800055100293 Package: Case [200 Units] In Commercial Distribution |
FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-08-18 |
Device Publish Date | 2020-08-10 |
28800055100467 | SC110 |
28800055100450 | SS201 |
28800055100443 | SS202 |
28800055100436 | SS203 |
28800055100429 | SS204 |
28800055100412 | SS205 |
28800055100405 | SS206 |
28800055100399 | SS207 |
28800055100382 | SS208 |
28800055100375 | SC101 |
28800055100368 | SC102 |
28800055100351 | SC103 |
28800055100344 | SC104 |
28800055100337 | SC105 |
28800055100320 | SC106 |
28800055100313 | SC107 |
28800055100306 | SC108 |
28800055100290 | SC109 |