DTPM

GUDID 16970429841632

Co-Innovation Biotech Co., Ltd

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• Primary Device ID: 16970429841632
• NIH Device Record Key: f0a73668-d22b-4473-8bc3-656ba9088f7e
• Commercial Distribution Discontinuation: 2023-12-08
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: DTPM
• Version Model Number: 16P
• 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: true
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970429841635 [Primary]
GS1	16970429841632 [Package]; Contains: 06970429841635; Package: [25 Units]; Discontinued: 2023-11-10; Not in Commercial Distribution
GS1	26970429841639 [Package]; Contains: 06970429841635; Package: [100 Units]; Discontinued: 2023-11-10; Not in Commercial Distribution
GS1	36970429841636 [Package]; Contains: 06970429841635; Package: [210 Units]; Discontinued: 2023-11-10; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153050

FDA Product Code

• DJC: Thin Layer Chromatography, Methamphetamine

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-12-18
• Device Publish Date: 2023-12-08

On-Brand Devices [DTPM]

• 16970429841632: 16P
• 16970429841342: 13P