FDA UDI In Commercial Distribution 🇺🇸 United States

Regard

DI: 10809160369487 · Model: 405218REG · MEDICAL ACTION INDUSTRIES INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Regard
Primary DI
10809160369487
Version / Model
405218REG
Company Name
MEDICAL ACTION INDUSTRIES INC.
Labeler DUNS
092364462
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-22
Public Version
1
Public Version Date
2022-05-02
Public Version Status
New
Public Device Record Key
804b46e4-ee5d-42fd-912b-cc217e85644a

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
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
LRS I.V. start kit

GMDN Terms

Code Name
33963 Peripheral intravenous catheterization support kit

Identifiers

Type ID
Package 20809160369484
Primary 10809160369487