FDA UDI In Commercial Distribution 🇺🇸 United States

KMEDIC

DI: 14026704722355 · Model: IPN014544 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
KMEDIC
Primary DI
14026704722355
Version / Model
IPN014544
Catalog Number
KM48302
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-16
Public Version
1
Public Version Date
2024-02-26
Public Version Status
New
Public Device Record Key
e2d05409-2d78-41f0-baa0-2e08082f5c59

Device Description

BONE COMPASS 8"

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
GFI OSTEOTOME, MANUAL

GMDN Terms

Code Name
33651 Manual goniometer

Identifiers

Type ID
Direct Marking 44026704722356
Previous 24026704278842
Primary 14026704722355

Customer Contacts

Device Sizes

Type Value Unit Text
Length 20.3 Centimeter