FDA UDI In Commercial Distribution 🇺🇸 United States

BP®

DI: 00889024320710 · Model: 07.00008.038 · ZIMMER SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BP®
Primary DI
00889024320710
Version / Model
07.00008.038
Company Name
ZIMMER SPINE, INC.
Labeler DUNS
787663400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-22
Public Version
4
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
95208fb7-a107-4adf-8f9d-ae32c213b881

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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00889024320710

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 19 Millimeter
Length 20 Millimeter