FDA UDI In Commercial Distribution 🇺🇸 United States

Verifine

DI: 00850011833735 · Model: BL-32G · Promisemed Medical Devices Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Verifine
Primary DI
00850011833735
Version / Model
BL-32G
Company Name
Promisemed Medical Devices Inc.
Labeler DUNS
114566189
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2023-08-18
Public Version
1
Public Version Date
2023-08-28
Public Version Status
New
Public Device Record Key
1bc65123-0231-48a7-acc2-804e97646fd5

Device Description

Blood Lancet is a sterile, handheld, sharply-pointed, non-mechanical, scalpel-like instrument intended to be used by a healthcare provider or patient self to manually puncture the skin to obtain a small blood specimen.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
61579 Blood lancet, single-use

Identifiers

Type ID
Package 10850011833732
Primary 00850011833735
Unit of Use 80850011833731

Premarket Submissions

Submission Number Supplement Number
K221368 000