FDA UDI In Commercial Distribution 🇺🇸 United States

Twist Lancet (23G)

DI: 06949517002012 · Model: LF-TL-23 · Shandong Lianfa Medical Plastic Products CO.,LTD
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
30

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
Twist Lancet (23G)
Primary DI
06949517002012
Version / Model
LF-TL-23
Company Name
Shandong Lianfa Medical Plastic Products CO.,LTD
Labeler DUNS
421330121
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2019-04-30
Public Version
3
Public Version Date
2024-04-01
Public Version Status
Update
Public Device Record Key
24862935-dc20-4821-bb5e-39f4facad661

Device Description

Sterile Lancet for Single Use (Bag of 30 lancets), Sterilized with Irradiation

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
QRL Multiple Use Blood Lancet For Single Patient Use Only

GMDN Terms

Code Name
61579 Blood lancet, single-use

Identifiers

Type ID
Primary 06949517002012
Unit of Use 56949517066040