FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 20612479188697 · Model: 520 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
McKesson
Primary DI
20612479188697
Version / Model
520
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2020-07-21
Public Version
2
Public Version Date
2021-04-21
Public Version Status
Update
Public Device Record Key
b1bb7c2f-ed62-4a96-b40c-f3f86ab2d850

Device Description

McKesson Ear Curette 4 mm Cup

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
Yes
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
JYG Curette, Ear

GMDN Terms

Code Name
63876 Endaural surgical curette, single-use

Identifiers

Type ID
Package 40612479188707
Primary 20612479188697
Unit of Use 10612479258898