Safety-Lancet Mini 28G 85.1015

GUDID 04038917167147

Sarstedt Aktiengesellschaft & Co.KG

Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use Manual blood lancing device, single-use

• Primary Device ID: 04038917167147
• NIH Device Record Key: 0c5a832c-1d0d-4155-b1b2-01e46150cb4c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Safety-Lancet Mini 28G
• Version Model Number: 85.1015
• Catalog Number: 85.1015
• Company DUNS: 388000270
• Company Name: Sarstedt Aktiengesellschaft & Co.KG
• Device Count: 200
• DM Exempt: true
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04038917085021 [Primary]
GS1	04038917167147 [Unit of Use]

FDA Product Code

• FMK: Single use only blood lancet with an integral sharps injury prevention feature

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: 2022-12-08
• Device Publish Date: 2022-11-30

Devices Manufactured by Sarstedt Aktiengesellschaft & Co.KG

• 04066916001858 - Microvette® 200 Z: 2024-06-19
• 04038917312417 - Tube 50ml, 115x28mm, PP: 2024-06-03
• 04038917314312 - Tube 50ml, 115x28mm, PP: 2024-06-03
• 04038917410021 - Tube 39 x 13: 2024-05-30
• 04038917364195 - Blood Culture Adapter LongNeck: 2024-05-06
• 04038917369961 - 10ml Yellow Cap: 2024-05-06
• 04038917418874 - Adapter sleeve: 2024-05-06
• 04038917992541 - 8,5 ml Urine Monovette: 2024-05-06