FDA UDI In Commercial Distribution 🇺🇸 United States

Walgreens

DI: 00311917123622 · Model: 02-2201 · WALGREEN CO.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Walgreens
Primary DI
00311917123622
Version / Model
02-2201
Company Name
WALGREEN CO.
Labeler DUNS
008965063
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-05
Public Version
1
Public Version Date
2022-12-13
Public Version Status
New
Public Device Record Key
01785476-6c6b-492d-bc48-ca9f0be24cbf

Device Description

Walgreens Lancing Device

Device Characteristics

Single Use
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QRL Multiple Use Blood Lancet For Single Patient Use Only

GMDN Terms

Code Name
37243 Manual blood lancing device, reusable

Identifiers

Type ID
Primary 00311917123622
Package 10311917123629

Customer Contacts

Phone
8009254733