De-/Recapper 900 Flex ID 90.2060.140

GUDID 04038917977852

Sarstedt Aktiengesellschaft & Co.KG

Laboratory container/microscope slide robotic transfer system IVD

• Primary Device ID: 04038917977852
• NIH Device Record Key: e6585089-bf96-4926-9319-551ee4031184
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: De-/Recapper 900 Flex ID
• Version Model Number: 90.2060.140
• Catalog Number: 90.2060.140
• Company DUNS: 388000270
• Company Name: Sarstedt Aktiengesellschaft & Co.KG
• Device Count: 1
• 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: false
• Lot Batch: false
• Serial Number: true
• 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

Customer Support Contacts

• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04038917977852 [Primary]

FDA Product Code

• LXG: EQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE

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: 2023-09-18
• Device Publish Date: 2023-09-08

Devices Manufactured by Sarstedt Aktiengesellschaft & Co.KG

• 04038917992428 - 8,5 ml Urine Monovette: 2024-11-04
• 04038917260015 - Tube 5 ml, 75 x 13 mm , PP: 2024-11-01
• 04038917405867 - Tube 3,5 ml: 2024-11-01
• 04038917242578 - Tube 50ml, 114x28mm, PP: 2024-10-24
• 04038917408578 - Tube 5ml, 75x13mm: 2024-10-01
• 04038917994040 - Micro tube 0.5ml with cap: 2024-10-01
• 04038917994088 - Micro tube 0.5ml, PP: 2024-10-01
• 04038917994163 - Micro tube 0.5ml, PP brown: 2024-10-01