FDA UDI In Commercial Distribution 🇺🇸 United States

Zutron Medical

DI: 00817658021659 · Model: ZUTR50523 · ZUTRON MEDICAL, L.L.C.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Zutron Medical
Primary DI
00817658021659
Version / Model
ZUTR50523
Catalog Number
ZUTR50523
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
2023-09-21
Public Version
1
Public Version Date
2023-09-29
Public Version Status
New
Public Device Record Key
bb8c4c11-b9d4-4751-a652-d584101c9e5e

Device Description

Check valve, normally closed, non-sterile

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OCX Endoscopic Irrigation/Suction System

GMDN Terms

Code Name
46102 Surgical irrigation tubing set, single-use

Identifiers

Type ID
Package 00817658021666
Primary 00817658021659

Customer Contacts

Phone
8773435873

Premarket Submissions

Submission Number Supplement Number
K181509 000