FDA UDI In Commercial Distribution 🇺🇸 United States

KAINOS+

DI: 04047844005675 · Model: Bone graft substitute, granules 2-3mm · SIGNUS Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KAINOS+
Primary DI
04047844005675
Version / Model
Bone graft substitute, granules 2-3mm
Catalog Number
K003NT
Company Name
SIGNUS Medizintechnik GmbH
Labeler DUNS
344203948
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
7
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
0e9d2379-970c-4f9b-9c16-8ab14e40a2b1

Device Description

KAINOS+ is a microporous and macroporous biphasic calcium phosphate ceramic consisting of 60% Hydroxyapatite (HA) and 40% beta-Tricalcium Phosphate (ß-TCP). KAINOS+ is available in various shapes and sizes. KAINOS+ may be used with physiolo-gical saline, patient’s own serum, whole blood, or bone marrow aspirate (BMA).

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
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
MQV Filler, Bone Void, Calcium Compound

GMDN Terms

Code Name
17751 Bone matrix implant, synthetic, non-antimicrobial

Identifiers

Type ID
Primary 04047844005675

Customer Contacts

Phone
+49602391660

Premarket Submissions

Submission Number Supplement Number
K090387 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 1x10cm³

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 35 Degrees Celsius