FDA UDI In Commercial Distribution 🇺🇸 United States

OsteoMed

DI: 00845694011907 · Model: 380-0006 · OSTEOMED LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OsteoMed
Primary DI
00845694011907
Version / Model
380-0006
Catalog Number
380-0006
Company Name
OSTEOMED LLC
Labeler DUNS
606417780
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-17
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
d22a6f2b-377a-4872-bfbd-bf25aa80ed2c

Device Description

KobyGard, Single-Use Blades, Sterile

Device Characteristics

Single Use
Yes
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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWC Screw, fixation, bone

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00845694011907

Customer Contacts

Phone
+1(800)456-7779 ext. 1

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Sterile packaged blades should be stored at controlled room temperature.