FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 10612479213866 · Model: 16-M1616 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
McKesson
Primary DI
10612479213866
Version / Model
16-M1616
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-09
Public Version
10
Public Version Date
2023-03-31
Public Version Status
Update
Public Device Record Key
1159b9bf-2d31-41b5-94a6-080c455c71b2

Device Description

Catheter Urethral Male 16" 16FR

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GBM Catheter, Urethral
EZD Catheter, Straight

GMDN Terms

Code Name
34917 Indwelling urethral drainage balloon catheter, non-antimicrobial

Identifiers

Type ID
Primary 10612479213866
Package 20612479213870
Package 40612479213881