FDA UDI In Commercial Distribution 🇺🇸 United States

LANZO Lancing Device

DI: 00015482570156 · Model: 570015 · ARKRAY USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LANZO Lancing Device
Primary DI
00015482570156
Version / Model
570015
Company Name
ARKRAY USA, INC.
Labeler DUNS
008171162
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-30
Public Version
1
Public Version Date
2018-11-30
Public Version Status
New
Public Device Record Key
70e889e2-450d-4d88-8a19-b5cea240a408

Device Description

A hand-held manual instrument intended to be used for controlled skin puncture to obtain a capillary blood specimen (e.g., performed by a diabetic patient) typically at the fingertip or ear lobe. It is used with a sterile, disposable lancet tip, and has a manually-powered mechanism (e.g., spring-loaded) which enables the tip to puncture to a predetermined depth and blood subsequently to be squeezed out of the puncture site. This is a reusable device.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
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
No
Sterilization Prior Use
No

Product Codes

Code Name
FMK Lancet, Blood

GMDN Terms

Code Name
37243 Manual blood lancing device, reusable

Identifiers

Type ID
Primary 00015482570156

Customer Contacts