FDA UDI In Commercial Distribution 🇺🇸 United States

OsteoBallast

DI: 10889981232153 · Model: 56110000 · ISOTIS ORTHOBIOLOGICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OsteoBallast
Primary DI
10889981232153
Version / Model
56110000
Catalog Number
56110000
Company Name
ISOTIS ORTHOBIOLOGICS, INC.
Labeler DUNS
801089152
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-30
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
58c99011-3a78-4eb2-9a6f-9f61678fddc6

Device Description

OsteoBallast®, 150x11mm, 2-pack

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
No
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
44688 Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable

Identifiers

Type ID
Primary 10889981232153

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K200290 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 25 Degrees Celsius