Primary Device ID | 30351688074458 |
NIH Device Record Key | c413d00e-ecea-40c3-a8f9-b5078506621f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Clint Pharmaceuticals |
Version Model Number | ACL5SPG |
Company DUNS | 609197785 |
Company Name | CLINT PHARMACEUTICALS, INC. |
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 | true |
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 | 20351688074451 [Primary] |
GS1 | 30351688074458 [Package] Contains: 20351688074451 Package: CASE [30 Units] In Commercial Distribution |
CAZ | Anesthesia conduction kit |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-07-22 |
Device Publish Date | 2017-01-13 |
30351688073642 | ACL4EX |
30351688071761 | ACS22Q45 |
30351688071754 | ACL6SP45 |
30351688070184 | ACL7SP |
30351688069973 | ACS22Q35 |
30351688069492 | ACL10SPG |
30351688064084 | ACL12 |
30351688063254 | ACL10 |
30351688062325 | ACL1 |
30351688081289 | ACL11CH |
30351688080152 | ACL11RX |
30351688079545 | ACL11SPS12 |
30351688079538 | ACL10SPS12 |
30351688077985 | ACL17SPG |
30351688077213 | ACL5SPS |
30351688077091 | ACL14 |
30351688077046 | ACS22Q554 |
30351688077039 | ACS22Q354 |
30351688076742 | ACL6TG |
30351688076148 | ACL7SPG |
30351688076131 | ACL10AT |
30351688074502 | ACS22QQQ35 |
30351688074496 | ACL11SPS |
30351688074472 | ACL10SPS |
30351688074458 | ACL5SPG |
30351688073963 | ACS25Q35F |