FDA UDI In Commercial Distribution 🇺🇸 United States

CVS

DI: 00050428167274 · Model: CVS739091V2 · WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

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Basic Information

Brand Name
CVS
Primary DI
00050428167274
Version / Model
CVS739091V2
Catalog Number
CVS739091V2
Company Name
WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Labeler DUNS
062312574
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2026-04-09
Public Version
1
Public Version Date
2026-04-17
Public Version Status
New
Public Device Record Key
50cbf091-c20e-487e-b1c7-42680787972b

Device Description

Lancing Device, For Capillary Blood Sampling, 30G

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
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
Yes
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
61578 Manual blood lancing device, single-use

Identifiers

Type ID
Package 20504281672740
Primary 00050428167274
Unit of Use 80504281672742

Device Sizes

Type Value Unit Text
Device Size Text, specify 30 Gauge

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a dry and well ventilated room and not be mixed with virulent, harmful or corrosion materials.