FDA UDI In Commercial Distribution 🇺🇸 United States

Neoscope

DI: 00851545007470 · Model: NDS 35 · PROSURG INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Neoscope
Primary DI
00851545007470
Version / Model
NDS 35
Company Name
PROSURG INC
Labeler DUNS
188684609
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2020-04-22
Public Version Status
Update
Public Device Record Key
c6f431e3-bb1b-4fff-922a-be90c8c7eb85

Device Description

NEO-CYSTOSCOPE , DIAGNOSTIC SHEATH

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
FAJ Cystoscope And Accessories, Flexible/Rigid

GMDN Terms

Code Name
37084 Rigid endoscope telescope

Identifiers

Type ID
Primary 00851545007470
Package 10851545007477

Customer Contacts

Phone
408 945 4044

Premarket Submissions

Submission Number Supplement Number
K120766 000

Device Sizes

Type Value Unit Text
Outer Diameter 3.5 Millimeter