FDA UDI In Commercial Distribution 🇺🇸 United States

Easy Mini Eject Lancing Device

DI: 00891237001171 · Model: LF-LDE · HOME AIDE DIAGNOSTICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Easy Mini Eject Lancing Device
Primary DI
00891237001171
Version / Model
LF-LDE
Catalog Number
1171
Company Name
HOME AIDE DIAGNOSTICS, INC.
Labeler DUNS
783518983
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-03
Public Version
2
Public Version Date
2022-11-29
Public Version Status
Update
Public Device Record Key
0b0e28af-0a81-4be5-846b-1ea94835ab4d

Device Description

• Step-by-step instructions to acquire capillary blood sample. • Adjustable penetration depth • Maximum comfort • For use with most lancets

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FMK Lancet, Blood

GMDN Terms

Code Name
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Package 10891237001178
Primary 00891237001171

Customer Contacts

Phone
18009150116