FDA UDI In Commercial Distribution 🇺🇸 United States

Mckesson

DI: 10612479217444 · Model: 22-ESRE · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Mckesson
Primary DI
10612479217444
Version / Model
22-ESRE
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-19
Public Version
1
Public Version Date
2020-08-27
Public Version Status
New
Public Device Record Key
ccac9709-1863-4e6a-898f-07f967258cc9

Device Description

PAD, DISP SPLIT W/O CORD ADLT

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
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
42551 Electrosurgical return electrode, reusable

Identifiers

Type ID
Package 20612479217458
Primary 10612479217444

Premarket Submissions

Submission Number Supplement Number
K092761 000