Clint Pharmaceuticals

GUDID 30351688074502

CLINT PHARMACEUTICALS, INC.

Epidural anaesthesia set, non-medicated
Primary Device ID30351688074502
NIH Device Record Keyd6708f77-b93f-4be6-8517-7c86bfa87be1
Commercial Distribution Discontinuation2019-08-13
Commercial Distribution StatusNot in Commercial Distribution
Brand NameClint Pharmaceuticals
Version Model NumberACS22QQQ35
Company DUNS609197785
Company NameCLINT PHARMACEUTICALS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS120351688074505 [Primary]
GS130351688074502 [Package]
Contains: 20351688074505
Package: Case [30 Units]
Discontinued: 2019-08-13
Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

CAZAnesthesia conduction kit

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2019-11-08
Device Publish Date2017-01-13

On-Brand Devices [Clint Pharmaceuticals]

30351688073642ACL4EX
30351688071761ACS22Q45
30351688071754ACL6SP45
30351688070184ACL7SP
30351688069973ACS22Q35
30351688069492ACL10SPG
30351688064084ACL12
30351688063254ACL10
30351688062325ACL1
30351688081289ACL11CH
30351688080152ACL11RX
30351688079545ACL11SPS12
30351688079538ACL10SPS12
30351688077985ACL17SPG
30351688077213ACL5SPS
30351688077091ACL14
30351688077046ACS22Q554
30351688077039ACS22Q354
30351688076742ACL6TG
30351688076148ACL7SPG
30351688076131ACL10AT
30351688074502ACS22QQQ35
30351688074496ACL11SPS
30351688074472ACL10SPS
30351688074458ACL5SPG
30351688073963ACS25Q35F

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