ImCap Seal

GUDID 05060169691124

IMMUNODIAGNOSTIC SYSTEMS LIMITED

Test tube rack

• Primary Device ID: 05060169691124
• NIH Device Record Key: c35013d8-231a-461e-b173-161af8d77406
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ImCap Seal
• Version Model Number: CQ-Seal
• Company DUNS: 494268600
• Company Name: IMMUNODIAGNOSTIC SYSTEMS LIMITED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +4401915190660
• Email: info.uk@idsplc.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060169691124 [Primary]

FDA Product Code

• LXG: Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-04-01

Devices Manufactured by IMMUNODIAGNOSTIC SYSTEMS LIMITED

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• 05060169696013 - IDS Beta CrossLaps® (CTX-I) Calibrator Set: 2024-01-11
• 05060169696051 - IDS Beta CrossLaps® (CTX-I) Control Set: 2024-01-11
• 05060169696457 - IDS ACTH II: 2023-08-31
• 05060169696495 - IDS ACTH II Calibrator Set: 2023-08-31
• 05060169696532 - IDS ACTH II Control Set: 2023-08-31
• 05060169691148 - IDS-iSYS SDSpeed Calc: 2023-07-05
• 05060169691261 - IDS Androstenedione: 2023-07-05