FDA UDI In Commercial Distribution 🇺🇸 United States

OSTEOPAL®

DI: 04260102130494 · Model: V · Heraeus Medical GmbH
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
OSTEOPAL®
Primary DI
04260102130494
Version / Model
V
Catalog Number
66031896
Company Name
Heraeus Medical GmbH
Labeler DUNS
333623937
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-10
Public Version
1
Public Version Date
2020-08-18
Public Version Status
New
Public Device Record Key
ce596653-402c-44ef-a9ff-7bf008216078

Device Description

Osteopal® V is an acrylic cement for use in vertebroplasty and kyphoplasty. It is formed from powder and liquid by exothermic polymerization

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LOD Bone Cement
NDN Cement, Bone, Vertebroplasty

GMDN Terms

Code Name
35217 Orthopaedic cement, non-antimicrobial

Identifiers

Type ID
Package 04260102130326
Primary 04260102130494
Package 04260102132283

Premarket Submissions

Submission Number Supplement Number
K050085 000