FDA UDI In Commercial Distribution 🇺🇸 United States

McKesson

DI: 10612479262475 · Model: 306617 · MCKESSON MEDICAL-SURGICAL INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
McKesson
Primary DI
10612479262475
Version / Model
306617
Company Name
MCKESSON MEDICAL-SURGICAL INC.
Labeler DUNS
023904428
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-11
Public Version
1
Public Version Date
2022-04-19
Public Version Status
New
Public Device Record Key
500e83e7-ad49-413d-b64e-e1c826e8d8f4

Device Description

Safety Hypodermic Needles GLIDE Thin Wall 21G x 1 in (50/bx, 10/cs)

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
59230 Hypodermic needle, single-use

Identifiers

Type ID
Package 20612479262489
Primary 10612479262475
Package 40612479262490

Premarket Submissions

Submission Number Supplement Number
K951254 000