FDA UDI In Commercial Distribution 🇺🇸 United States

Zutron Medical

DI: 00817658020164 · Model: ZUTR161700 · ZUTRON MEDICAL, L.L.C.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zutron Medical
Primary DI
00817658020164
Version / Model
ZUTR161700
Catalog Number
ZUTR161700
Company Name
ZUTRON MEDICAL, L.L.C.
Labeler DUNS
962532441
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-01
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
d5c10820-c01e-44ce-934d-83539e31c44c

Device Description

When added scope siffness is desired to negotiate a difficult colon, and prior to repositioning the patient, simply insert the Colonoscope Stiffening Device into the biopsy port to stiffen the insertion tube and advance to the cecum. The device is then withdrawn and the procedure is completed as usual. These reusable devices are compatible with Pentax ®, Fujinon®, Olympus® and Fuse® non-variable stiffness endoscopes.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "High-level Disinfectant", "Ethylene Oxide"]

Product Codes

Code Name
FDF Colonoscope And Accessories, Flexible/Rigid

GMDN Terms

Code Name
17826 Colonoscope stiffener

Identifiers

Type ID
Primary 00817658020164