FDA UDI In Commercial Distribution 🇺🇸 United States

KMEDIC

DI: 24026704286229 · Model: IPN015180 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
KMEDIC
Primary DI
24026704286229
Version / Model
IPN015180
Catalog Number
KM55370
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-15
Public Version
3
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
e07c6c78-7071-4107-b9a4-0b6e101a47d4

Device Description

IMPACTOR STANDARD OFFSET, 8 1/2"

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
Yes
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
HWA IMPACTOR

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 24026704286229
Direct Marking 04026704286225

Customer Contacts

Device Sizes

Type Value Unit Text
Length 21.6 Centimeter