Srew cap Tobe 10 ml with Stabilur tablet

GUDID 04038917203050

Sarstedt Aktiengesellschaft & Co.KG

General specimen container IVD, no additive/medium

• Primary Device ID: 04038917203050
• NIH Device Record Key: df04e2c1-2bce-4fcb-96fa-0df8a32ea128
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Srew cap Tobe 10 ml with Stabilur tablet
• Version Model Number: 51.1543.004
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04038917159647 [Primary]
GS1	04038917203050 [Unit of Use]

FDA Product Code

• NNK: Container, Specimen Mailer And Storage, Non-Sterile

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: 2024-11-26
• Device Publish Date: 2024-11-18

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