FDA UDI In Commercial Distribution 🇺🇸 United States

KMEDIC

DI: 24026704286274 · Model: IPN015185 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
KMEDIC
Primary DI
24026704286274
Version / Model
IPN015185
Catalog Number
KM55375
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
bedb2a3b-882a-4780-bb9a-d928b300986d

Device Description

GRAFT DRIVER LUMBAR GUARDED, 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
HAO INSTRUMENT, SURGICAL, NON-POWERED

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 24026704286274
Direct Marking 04026704286270

Customer Contacts

Device Sizes

Type Value Unit Text
Length 21.6 Centimeter
Width 10 Millimeter