Co-innovation

GUDID 06970429840218

Co-Innovation Biotech Co., Ltd

Total human chorionic gonadotropin (HCG) IVD, kit, immunochromatographic test (ICT), rapid Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical

• Primary Device ID: 06970429840218
• NIH Device Record Key: 98c205c4-cd7a-42d1-80d9-806caeeb0ce6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Co-innovation
• Version Model Number: HCG Strip/4.0mm
• Company DUNS: 421302978
• Company Name: Co-Innovation Biotech Co., Ltd
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970429840102 [Primary]
GS1	06970429840201 [Package]; Contains: 06970429840102; Package: [100 Units]; In Commercial Distribution
GS1	06970429840218 [Package]; Contains: 06970429840201; Package: [100 Units]; In Commercial Distribution

FDA Product Code

• LCX: Kit, Test, Pregnancy, Hcg, Over The Counter

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: 2017-03-23

On-Brand Devices [Co-innovation]

• 06970429841420: 14P DRUG TEST CUP
• 16970429841410: 14P Rapid Multi-Drug Test Cup
• 26970429841288: 12P drug test cup
• 36970429841278: 12P Drug Test Dipcard
• 36970429841261: 12P DRUG TEST DIPCARD
• 16970429841250: 12P Rapid Multi-Drug Test Cup
• 26970429841110: Rapid Multi drug Test Cup 11 Pannel
• 16970429840710: 7P Rapid Multi-Drug Test Cup
• 16970429840635: Rapid ETG Test Dipcard
• 36970429840622: 6P Drug Test Dipcard
• 06970429840539: Rapid THC Test Dipcard
• 06970429840614: THC Strip/3.0mm
• 06970429840423: OPI Test Strip
• 06970429840317: 3P Drug Test Dipcard
• 06970429840416: HCG Cassette
• 06970429840218: HCG Strip/4.0mm
• 16970429841618: 16P CUP
• 16970429841908: 12P Drug Test
• 16970429841809: 18P Drug Test
• 16970429841700: 17P Drug Test
• 16970429841625: 16P Drug Test
• 16970429841533: 15P Drug Test
• 16970429841441: 14P Drug Test
• 16970429841816: Rapid Multi-drug Test Cup
• 16970429840178: HCG TEST