FDA UDI Not in Commercial Distribution 🇺🇸 United States

Pathway

DI: 00852423006332 · Model: N/A · PROMETHEUS GROUP OF NEW HAMPSHIRE LIMITED, THE
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Pathway
Primary DI
00852423006332
Version / Model
N/A
Catalog Number
N/A
Company Name
PROMETHEUS GROUP OF NEW HAMPSHIRE LIMITED, THE
Labeler DUNS
625863568
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-30
Public Version
3
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
945e8319-48d5-499c-b487-9b435e1ab202
Distribution End Date
2017-02-02

Device Description

Pathway® RealTime Ultrasound

Device Characteristics

Single Use
No
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
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYO System, Imaging, Pulsed Echo, Ultrasonic
ITX Transducer, Ultrasonic, Diagnostic

GMDN Terms

Code Name
35712 Ultrasonic lithotripsy system
37139 Ultrasonic lithotripsy system probe, reusable

Identifiers

Type ID
Primary 00852423006332

Customer Contacts