Safety-Lancet Normal 21G 85.1016

GUDID 04038917167154

Sarstedt Aktiengesellschaft & Co.KG

Manual blood lancing device, single-use

• Primary Device ID: 04038917167154
• NIH Device Record Key: 0082d635-8316-4c3e-a47f-6d54208f1104
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Safety-Lancet Normal 21G
• Version Model Number: 85.1016
• Catalog Number: 85.1016
• 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	04038917085038 [Primary]
GS1	04038917167154 [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

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