Medlance Plus safety lancet 7043

GUDID 05907506237105

Sterile,single-use safety lancets for capillary blood sampling.

HTL STREFA S A

Blood lancet, single-use

• Primary Device ID: 05907506237105
• NIH Device Record Key: b0f463d0-d4f6-4ca5-9b58-82401d90f58e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medlance Plus safety lancet
• Version Model Number: Lite, 25G x 1.5 mm
• Catalog Number: 7043
• Company DUNS: 422528088
• Company Name: HTL STREFA S A
• Device Count: 200
• 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

Customer Support Contacts

• Phone: +484227000010
• Email: info@htl-strefa.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05907506237105 [Primary]
GS1	15907506237102 [Package]; Package: shipper [10 Units]; In Commercial Distribution
GS1	85907506237101 [Unit of Use]

FDA Product Code

• FMK: Lancet, Blood

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: 2020-02-28
• Device Publish Date: 2020-02-20

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