Primary Device ID | 14571225315550 |
NIH Device Record Key | 42dcc6d4-db2c-4a6f-9ea4-053db1c77200 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | STERiJECT TM |
Version Model Number | PRE-30006 |
Company DUNS | 716217877 |
Company Name | TSK LABORATORY, JAPAN |
Device Count | 100 |
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 | false |
OTC Over-The-Counter | true |
Outer Diameter | 0.3 Millimeter |
Outer Diameter | 0.3 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04571225315539 [Unit of Use] |
GS1 | 04571225315553 [Primary] |
GS1 | 14571225315550 [Package] Contains: 04571225315553 Package: Carton [60 Units] In Commercial Distribution |
FMI | Needle, hypodermic, single lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2016-09-17 |
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