FDA UDI In Commercial Distribution 🇺🇸 United States

Safety Lancet (21G)

DI: 06949517001039 · Model: LF-PA-21 · Shandong Lianfa Medical Plastic Products CO.,LTD
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
Safety Lancet (21G)
Primary DI
06949517001039
Version / Model
LF-PA-21
Company Name
Shandong Lianfa Medical Plastic Products CO.,LTD
Labeler DUNS
421330121
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2019-04-30
Public Version
1
Public Version Date
2019-05-08
Public Version Status
New
Public Device Record Key
e5348312-5f28-49d1-837b-1643168ba607

Device Description

Pressure Activated Safety Lancet (Box of 25 lancets), sterilized with Ethylene Oxide

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMK Lancet, Blood

GMDN Terms

Code Name
61579 Blood lancet, single-use

Identifiers

Type ID
Primary 06949517001039
Unit of Use 56949517062035