FDA UDI In Commercial Distribution 🇺🇸 United States

IBIS XL

DI: 00822409034451 · Model: 752-8575-57A · Ortho Development Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IBIS XL
Primary DI
00822409034451
Version / Model
752-8575-57A
Company Name
Ortho Development Corporation
Labeler DUNS
876542390
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-31
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
1b8dbcb0-2632-432e-9821-6000a2498a81

Device Description

Diameter 8.5 x 75 mm Cannulated Polyaxial Screw

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
Yes
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
NKB Thoracolumbosacral pedicle screw system

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00822409034451

Customer Contacts

Device Sizes

Type Value Unit Text
Length 75 Millimeter
Outer Diameter 8.5 Millimeter