FDA UDI In Commercial Distribution 🇺🇸 United States

Uscope

DI: 06971176280029 · Model: PU3022A · Zhuhai Pusen Medical Technology Co, Ltd
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Uscope
Primary DI
06971176280029
Version / Model
PU3022A
Company Name
Zhuhai Pusen Medical Technology Co, Ltd
Labeler DUNS
544427443
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-12
Public Version
5
Public Version Date
2022-12-06
Public Version Status
Update
Public Device Record Key
0967ca09-326c-4f68-9be5-18eca4c4c2d2

Device Description

This instrument has been designed to be used with endo-therapy accessories such as a biopsy forceps and other ancillary equipment for endoscopy and endoscopic surgery within urinary tract and interior of the kidney. This instrument is labeled Reverse Deflection.

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
Yes
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FGB Ureteroscope And Accessories, Flexible/Rigid

GMDN Terms

Code Name
64074 Flexible video ureteroscope, single-use

Identifiers

Type ID
Package 16971176280026
Primary 06971176280029

Premarket Submissions

Submission Number Supplement Number
K172098 000