FDA UDI In Commercial Distribution 🇺🇸 United States

KMEDIC

DI: 14026704722362 · Model: IPN015737 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
KMEDIC
Primary DI
14026704722362
Version / Model
IPN015737
Catalog Number
KM71009
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-27
Public Version
1
Public Version Date
2023-07-05
Public Version Status
New
Public Device Record Key
ffd2237d-f545-4871-aeb3-6fdaba91a50d

Device Description

K-WIRE STEINMANN CASE-9" K-WIRE & PINS

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
62868 Medical capital equipment storage bag/case

Identifiers

Type ID
Primary 14026704722362
Previous 24026704292275

Customer Contacts

Device Sizes

Type Value Unit Text
Width 5.5 Inch
Length 19.5 Inch
Depth 2.5 Inch