Tube 39 x 13

GUDID 04038917410021

Sarstedt Aktiengesellschaft & Co.KG

General specimen container IVD, no additive/medium

• Primary Device ID: 04038917410021
• NIH Device Record Key: a43752cb-b3de-4d70-abaf-acf0fb2b27f8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tube 39 x 13
• Version Model Number: 72.693.060
• Company DUNS: 388000270
• Company Name: Sarstedt Aktiengesellschaft & Co.KG
• Device Count: 2500
• 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: false
• 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	04038917410021 [Unit of Use]
GS1	04038917432146 [Primary]

FDA Product Code

• KDT: Container, Specimen Mailer And Storage, Sterile

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-30
• Device Publish Date: 2024-05-22

Devices Manufactured by Sarstedt Aktiengesellschaft & Co.KG

• 04038917310949 - Biosphere® screw cap, white: 2025-08-04
• 04038917326698 - Biosphere® Screw Cap, green: 2025-08-04
• 04038917328289 - Biosphere® screw cap, orange: 2025-08-04
• 04038917369909 - Biosphere® Screw Cap, red: 2025-08-04
• 04038917411769 - Biosphere® screw cap, yellow: 2025-08-04
• 04038917411790 - Biosphere® Screw Cap, violet: 2025-08-04
• 04038917411820 - Biosphere® Screw Cap, blue: 2025-08-04
• 04038917411851 - Biosphere® Screw Cap, black: 2025-08-04