FDA UDI In Commercial Distribution 🇺🇸 United States

FORA

DI: 00816042012037 · Model: LANCING DEVICE · FORA CARE INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FORA
Primary DI
00816042012037
Version / Model
LANCING DEVICE
Company Name
FORA CARE INC.
Labeler DUNS
004340807
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-09
Public Version
1
Public Version Date
2023-06-19
Public Version Status
New
Public Device Record Key
004d89ca-52b6-456b-ae4b-841ac92740a8

Device Description

LANCING DEVICE with AST Cap

Device Characteristics

Single Use
No
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
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 00816042012037

Premarket Submissions

Submission Number Supplement Number
K221419 000