FDA UDI In Commercial Distribution 🇺🇸 United States

PRO-NOX™

DI: 10889483300381 · Model: WES-PROLRGKIT · SUNMED, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
PRO-NOX™
Primary DI
10889483300381
Version / Model
WES-PROLRGKIT
Catalog Number
WES-PROLRGKIT
Company Name
SUNMED, LLC
Labeler DUNS
069009268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-12
Public Version
1
Public Version Date
2026-01-20
Public Version Status
New
Public Device Record Key
59693d78-9a80-419e-a5d4-c2443d038e30

Device Description

Pro-Nox Small Adult Disposable Kit Patient Circuit, 77" Magenta Tubing, Large Mask

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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CAH Filter, Bacterial, Breathing-Circuit

GMDN Terms

Code Name
37704 Anaesthesia breathing circuit, single-use

Identifiers

Type ID
Package 20889483300388
Primary 10889483300381
Previous 00709078006692

Customer Contacts