Pipette tip 1250 µl XL

GUDID 04066916023065

Sarstedt Aktiengesellschaft & Co.KG

User-induced pipette

• Primary Device ID: 04066916023065
• NIH Device Record Key: 4bc8aa74-4458-4236-aea4-79ffe1e7c52a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pipette tip 1250 µl XL
• Version Model Number: 70.3070.200
• Company DUNS: 388000270
• Company Name: Sarstedt Aktiengesellschaft & Co.KG
• Device Count: 480
• 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	04066916022952 [Primary]
GS1	04066916023065 [Unit of Use]

FDA Product Code

• JRC: Micro Pipette

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: 2025-02-28
• Device Publish Date: 2025-02-20

On-Brand Devices [Pipette tip 1250 µl XL]

• 04038917434652: 70.3060
• 04038917432481: 70.3060.305
• 04038917432399: 70.3060.205
• 04038917432368: 70.3060.210
• 04038917432337: 70.3060.200
• 04038917432245: 70.3060.110
• 04038917432214: 70.3060.100
• 04066916023065: 70.3070.200
• 04066916022907: 70.3070.205