Acti-Lance, safety lancet

Basic Information

• Brand Name: Acti-Lance, safety lancet
• Primary DI: 00859135002492
• Version / Model: Universal, 23G
• Catalog Number: 7312
• Company Name: HTL STREFA S A
• Labeler DUNS: 422528088
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 25
• Record Status: Published
• Publish Date: 2021-06-06
• Public Version: 1
• Public Version Date: 2021-06-14
• Public Version Status: New
• Public Device Record Key: eee9dec2-f46d-4aa9-b470-a783d678a52c

Device Description

Safety lancets are sterile, single use medical devices intended for capillary blood sampling.

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• Over the Counter (OTC): Yes
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: Yes
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
FMK	Lancet, Blood	General, Plastic Surgery	878.4850	2

GMDN Terms

Code	Name	Definition	Implantable	Status
61579	Blood lancet, single-use	A sterile, hand-held, sharply-pointed, non-mechanical, scalpel-like instrument intended to be used by a healthcare provider to manually puncture the skin of a patient to obtain a small blood specimen or drain a cyst or boil. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Unit of Use	80859135002498	GS1
Primary	00859135002492	GS1
Package	10859135002499	GS1	Shipper box	45	In Commercial Distribution

Customer Contacts

• Phone: [phone]
• Email: [email protected]