FDA UDI In Commercial Distribution 🇺🇸 United States

HemaSource

DI: 00853614008685 · Model: BLC2128 · Hemasource, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
HemaSource
Primary DI
00853614008685
Version / Model
BLC2128
Company Name
Hemasource, Inc.
Labeler DUNS
009046405
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
25713038-ef6c-41a0-957a-816510ea7835

Device Description

Lancet 21G 2.8mm Dual Spring

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
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 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 10853614008682
Primary 00853614008685

Premarket Submissions

Submission Number Supplement Number
K222090 000