FDA UDI In Commercial Distribution 🇺🇸 United States

n/a

DI: 00822409097982 · Model: 651-3709 · Ortho Development Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
n/a
Primary DI
00822409097982
Version / Model
651-3709
Company Name
Ortho Development Corporation
Labeler DUNS
876542390
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-25
Public Version
1
Public Version Date
2022-03-07
Public Version Status
New
Public Device Record Key
f6159e80-462d-4f5b-a7a1-bc5d1dcc47b4

Device Description

Vusion OS Parallel Trials 11x9x30mm

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 00822409097982

Customer Contacts

Device Sizes

Type Value Unit Text
Height 30 Millimeter
Width 11 Millimeter
Length 9 Millimeter