FDA UDI In Commercial Distribution 🇺🇸 United States

FORZA

DI: 18257200022144 · Model: 87-1208SP · Orthofix US LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FORZA
Primary DI
18257200022144
Version / Model
87-1208SP
Company Name
Orthofix US LLC
Labeler DUNS
927083808
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-01
Public Version
4
Public Version Date
2023-02-16
Public Version Status
Update
Public Device Record Key
81232167-0b65-4350-b233-bb3540382a3b

Device Description

11W X 27L X 8H, 4DEG STRAIGHT IMPLANT, STERILE

Device Characteristics

Single Use
No
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
Yes
PM Exempt
Yes
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
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 18257200022144

Customer Contacts