FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 40612479224856 · Model: 314 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
McKesson
Primary DI
40612479224856
Version / Model
314
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-09
Public Version
2
Public Version Date
2021-01-08
Public Version Status
Update
Public Device Record Key
9c1a1a29-8371-4bd0-a15a-7d2437279719

Device Description

Exam Light 12 INCH GOOSENECK | CHROME 34 in – 72 in

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KZF Device, Medical Examination, Ac Powered

GMDN Terms

Code Name
36843 Mobile examination/treatment room light

Identifiers

Type ID
Primary 40612479224856