FDA UDI In Commercial Distribution 🇺🇸 United States

Peripheral ROTAPRO™

DI: 00191506007119 · Model: H749395141250 · BOSTON SCIENTIFIC CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Peripheral ROTAPRO™
Primary DI
00191506007119
Version / Model
H749395141250
Catalog Number
H749395141250
Company Name
BOSTON SCIENTIFIC CORPORATION
Labeler DUNS
021717889
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-16
Public Version
1
Public Version Date
2022-09-26
Public Version Status
New
Public Device Record Key
eb00638d-fada-4e08-9fbe-9222321fc754

Device Description

Rotational Atherectomy Device

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MCW Catheter, peripheral, atherectomy

GMDN Terms

Code Name
61205 Mechanical atherectomy system, coronary, line-powered

Identifiers

Type ID
Primary 00191506007119

Device Sizes

Type Value Unit Text
Atherectomy Rotating Component Diameter 1.25 Millimeter