FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 00612479259812 · Model: 16-DC3 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
McKesson
Primary DI
00612479259812
Version / Model
16-DC3
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-30
Public Version
1
Public Version Date
2021-04-07
Public Version Status
New
Public Device Record Key
deabb75f-797a-4f67-80db-25389c81a3ec

Device Description

CURETTE, DERMAL DISP 3MM

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FZS Curette, Surgical, General Use

GMDN Terms

Code Name
63259 Dermal curette

Identifiers

Type ID
Package 00612479259829
Primary 00612479259812
Package 00612479259836