FDA UDI In Commercial Distribution 🇺🇸 United States

K2M General Instruments

DI: 10888857574151 · Model: PRO-1361-30 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
K2M General Instruments
Primary DI
10888857574151
Version / Model
PRO-1361-30
Catalog Number
PRO-1361-30
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-09
Public Version
1
Public Version Date
2024-02-19
Public Version Status
New
Public Device Record Key
8a7a89cb-e3d2-4ffe-a8c6-c3eb2bf53c22

Device Description

Parallel Trial Size 12x30x13 mm

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
44788 Spinal implant trial

Identifiers

Type ID
Primary 10888857574151

Customer Contacts

Device Sizes

Type Value Unit Text
Length 30 Millimeter
Height 13 Millimeter
Width 12 Millimeter