FDA UDI In Commercial Distribution 🇺🇸 United States

Regard™

DI: 10194717118701 · Model: HT01040F · ROI CPS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Regard™
Primary DI
10194717118701
Version / Model
HT01040F
Company Name
ROI CPS, LLC
Labeler DUNS
117174678
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-08
Public Version
1
Public Version Date
2024-02-16
Public Version Status
New
Public Device Record Key
f3a92a1f-b545-41a1-9f15-2cc8ac7b4b1f

Device Description

ANGIO KIT

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
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
OEQ Angiography/Angioplasty Kit

GMDN Terms

Code Name
16545 Angiography kit

Identifiers

Type ID
Package 20194717118708
Primary 10194717118701