Primary Device ID | 04063574200012 |
NIH Device Record Key | 1d3d2786-f0e8-4488-a3d8-76e7336fc925 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | nextaro® |
Version Model Number | 88353 |
Company DUNS | 315549311 |
Company Name | sfm medical devices GmbH |
Device Count | 1 |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04063574200012 [Primary] |
LHI | Set, I.V. Fluid Transfer |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-04-04 |
Device Publish Date | 2022-03-25 |
04063574100015 | nextaro® Transfer System (20/20 with 15 µm filter, nominal) |
04063574200012 | nextaro® Transfer System (20/20 with 15 µm filter, nominal) |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NEXTARO 79345253 not registered Live/Pending |
sfm medical devices GmbH 2022-06-01 |