FDA UDI In Commercial Distribution 🇺🇸 United States

K2M General Instruments

DI: 10888857494367 · Model: AG01-96102 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
K2M General Instruments
Primary DI
10888857494367
Version / Model
AG01-96102
Catalog Number
AG01-96102
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-20
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
48d31443-d362-4f57-83bb-a06e5e41355e

Device Description

Parallel Modular Trial, Size 18x60x16 mm, 0°

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
HWT TEMPLATE

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 10888857494367

Customer Contacts

Device Sizes

Type Value Unit Text
Height 16 Millimeter
Length 60 Millimeter
Width 18 Millimeter