Primary Device ID | 00616784703824 |
NIH Device Record Key | 2ef8f650-c6b1-4305-96ed-ad19d9768fb4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IV Administration Set |
Version Model Number | 7038 |
Company DUNS | 008124539 |
Company Name | DYNAREX CORPORATION |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00616784703824 [Primary] |
FPA | Set, Administration, Intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-12-11 |
Device Publish Date | 2018-01-06 |
00616787704729 | 7047 |
00616784705330 | 7053 |
00616784705231 | 7052 |
00616784705132 | 7051 |
00616784705033 | 7050 |
00616784704937 | 7049 |
00616784704838 | 7048 |
00616784704524 | 7045 |
00616784704425 | 7044 |
00616784704326 | 7043 |
00616784703923 | 7039 |
00616784703824 | 7038 |
00616784703732 | 7037 |
00616784703633 | 7036 |
00616784703534 | 7035 |
00616784703435 | 7034 |
00616784703336 | 7033 |
00616784703237 | 7032 |
00616784703138 | 7031 |
00616784703039 | 7030 |
00616784704739 | 7047 |