FDA UDI In Commercial Distribution 🇺🇸 United States

Mckesson

DI: 20612479161546 · Model: 11-19611 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Mckesson
Primary DI
20612479161546
Version / Model
11-19611
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-10
Public Version
1
Public Version Date
2020-08-18
Public Version Status
New
Public Device Record Key
b3623b35-16c9-4e1a-a0b6-0bba91689c06

Device Description

GYNECATH H/S CATHETER 7FR (10/

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
No
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
LKF Cannula, Manipulator/Injector, Uterine

GMDN Terms

Code Name
34157 Salpingographic catheter

Identifiers

Type ID
Package 30612479162489
Primary 20612479161546
Package 40612479161588

Premarket Submissions

Submission Number Supplement Number
K961752 000