ImCap Seal

GUDID 05060169691124

IMMUNODIAGNOSTIC SYSTEMS LIMITED

Test tube rack
Primary Device ID05060169691124
NIH Device Record Keyc35013d8-231a-461e-b173-161af8d77406
Commercial Distribution StatusIn Commercial Distribution
Brand NameImCap Seal
Version Model NumberCQ-Seal
Company DUNS494268600
Company NameIMMUNODIAGNOSTIC SYSTEMS LIMITED
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+4401915190660
Emailinfo.uk@idsplc.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105060169691124 [Primary]

FDA Product Code

LXGEquipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-04-01

Devices Manufactured by IMMUNODIAGNOSTIC SYSTEMS LIMITED

05060169695986 - IDS Beta CrossLaps® (CTX-I)2024-01-11
05060169696013 - IDS Beta CrossLaps® (CTX-I) Calibrator Set2024-01-11
05060169696051 - IDS Beta CrossLaps® (CTX-I) Control Set2024-01-11
05060169696457 - IDS ACTH II2023-08-31
05060169696495 - IDS ACTH II Calibrator Set2023-08-31
05060169696532 - IDS ACTH II Control Set2023-08-31
05060169691148 - IDS-iSYS SDSpeed Calc2023-07-05
05060169691261 - IDS Androstenedione2023-07-05

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