Primary Device ID | 00616784700731 |
NIH Device Record Key | 571189fa-5f13-463f-b55a-384b6cca7fe8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Syringe w/Needle |
Version Model Number | 7007 |
Company DUNS | 008124539 |
Company Name | DYNAREX CORPORATION |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00616784700717 [Unit of Use] |
GS1 | 00616784700724 [Primary] |
GS1 | 00616784700731 [Package] Contains: 00616784700724 Package: [4 Units] In Commercial Distribution |
FMF | Syringe, Piston |
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 | 2016-09-24 |
00616784701639 | 7016 |
00616784701530 | 7015 |
00616784701431 | 7014 |
00616784701332 | 7013 |
00616784701233 | 7012 |
00616784701134 | 7011 |
00616784701035 | 7010 |
00616784700939 | 7009 |
00616784700830 | 7008 |
00616784700731 | 7007 |
00616784700632 | 7006 |
00616784700533 | 7005 |
00616784700434 | 7004 |
00616784700335 | 7003 |
00616784700236 | 7002 |
00616784700137 | 7001 |
00616784700038 | 7000 |
00616784699936 | 6999 |
00616784699837 | 6998 |
00616784699738 | 6997 |
00616784699639 | 6996 |
00616784699530 | 6995 |
00616784699431 | 6994 |