FDA UDI Not in Commercial Distribution 🇺🇸 United States

CONVERTORS

DI: 50885380074026 · Model: KC1230778 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
200

Basic Information

Brand Name
CONVERTORS
Primary DI
50885380074026
Version / Model
KC1230778
Catalog Number
KC1230778
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2016-06-21
Public Version
5
Public Version Date
2022-03-07
Public Version Status
Update
Public Device Record Key
dfd1cd53-7b63-4f0e-af92-9577793b2d74
Distribution End Date
2022-03-06

Device Description

Medium Irrigation Pouch BNS

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
KKX Drape, surgical

GMDN Terms

Code Name
47782 Patient surgical drape, single-use, non-sterile

Identifiers

Type ID
Primary 50885380074026
Unit of Use 10885380074028