FDA UDI In Commercial Distribution 🇺🇸 United States

Dynamik Intervertebral Body Fusion Device

DI: 07640139342300 · Model: DYN-BS 22 12-S · SpineArt SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Dynamik Intervertebral Body Fusion Device
Primary DI
07640139342300
Version / Model
DYN-BS 22 12-S
Catalog Number
DYN-BS 22 12-S
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-12
Public Version
2
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
9a4a8845-17d4-4a5a-823f-e0045776eacf

Device Description

Bone Substitute L22 H12

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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

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

Identifiers

Type ID
Primary 07640139342300

Device Sizes

Type Value Unit Text
Length 22 Millimeter
Height 12 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius