FDA UDI In Commercial Distribution 🇺🇸 United States

OSTEOPORE TCP

DI: M505SC44220G0 · Model: SC44220G · KASIOS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OSTEOPORE TCP
Primary DI
M505SC44220G0
Version / Model
SC44220G
Company Name
KASIOS
Labeler DUNS
572720055
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-12
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
872397a5-2b43-4159-939e-f5bca873a6a9

Device Description

Phosphocalcic ceramic

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
No
PM Exempt
No
Has Serial Number
Yes
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
MQV Filler, Bone Void, Calcium Compound

GMDN Terms

Code Name
16966 Synthetic bone graft

Identifiers

Type ID
Primary M505SC44220G0

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 2-3 mm – 20 cc – 12,4 g