Microvette® 200 Z

GUDID 04066916001858

Sarstedt Aktiengesellschaft & Co.KG

Capillary blood transfer tube IVD, clot activator

• Primary Device ID: 04066916001858
• NIH Device Record Key: bdf74f02-3c4e-4f35-9d6e-788bad81cc87
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Microvette® 200 Z
• Version Model Number: 20.1290.200
• Company DUNS: 388000270
• Company Name: Sarstedt Aktiengesellschaft & Co.KG
• Device Count: 100
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04066916001858 [Unit of Use]
GS1	04066916001865 [Primary]

FDA Product Code

• GIO: Tube, Collection, Capillary Blood

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: 2024-06-19
• Device Publish Date: 2024-06-11

On-Brand Devices [Microvette® 200 Z]

• 04038917895774: 20.1290.899
• 04038917201254: 201290100
• 04066916001858: 20.1290.200