FDA UDI In Commercial Distribution 🇺🇸 United States

K2M General Instruments

DI: 10888857558656 · Model: PRO-1279-06 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
K2M General Instruments
Primary DI
10888857558656
Version / Model
PRO-1279-06
Catalog Number
PRO-1279-06
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-07
Public Version
1
Public Version Date
2023-02-15
Public Version Status
New
Public Device Record Key
4cef6d05-5009-458f-b76a-81f9338df2a0

Device Description

Lordotic Rasp Size 22x30x20 mm, 4 Deg

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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 10888857558656

Customer Contacts

Device Sizes

Type Value Unit Text
Width 30 Millimeter
Height 20 Millimeter
Angle 4 degree
Length 22 Millimeter