FDA UDI In Commercial Distribution 🇺🇸 United States

HemoCue Safety Lancet

DI: 04580505780462 · Model: 130148 · ASAHI POLYSLIDER COMPANY,LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
200

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
HemoCue Safety Lancet
Primary DI
04580505780462
Version / Model
130148
Company Name
ASAHI POLYSLIDER COMPANY,LIMITED
Labeler DUNS
718296825
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2022-11-30
Public Version
1
Public Version Date
2022-12-08
Public Version Status
New
Public Device Record Key
3d9248b6-f17b-4e78-a41e-5519c105bbed

Device Description

Box of 200 Sterile Single-Use Lancing Device 23 Gauge

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
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
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

GMDN Terms

Code Name
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Unit of Use 84580505780659
Primary 04580505780462

Device Sizes

Type Value Unit Text
Needle Gauge 23 Gauge