FDA UDI In Commercial Distribution 🇺🇸 United States

Autotome™ Pro RX 39

DI: 00191506039233 · Model: M00584390 · BOSTON SCIENTIFIC CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Autotome™ Pro RX 39
Primary DI
00191506039233
Version / Model
M00584390
Catalog Number
M00584390
Company Name
BOSTON SCIENTIFIC CORPORATION
Labeler DUNS
021717889
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-25
Public Version
1
Public Version Date
2023-11-02
Public Version Status
New
Public Device Record Key
53b75277-38e0-4463-b879-a3555d584018

Device Description

Cannulating Sphincterotome

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
KNS Unit, electrosurgical, endoscopic (with or without accessories)

GMDN Terms

Code Name
65185 ERCP catheter, non-balloon, electrosurgical

Identifiers

Type ID
Primary 00191506039233

Device Sizes

Type Value Unit Text
Device Size Text, specify 1.3mm Tip diameter
Device Size Text, specify 3.9F Tip diameter
Device Size Text, specify 25mm cut wire with insulation