FDA UDI In Commercial Distribution 🇺🇸 United States

Viceroy

DI: 08800039826358 · Model: A · DIOMEDICAL CO.,LTD.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Viceroy
Primary DI
08800039826358
Version / Model
A
Catalog Number
V-0202 090
Company Name
DIOMEDICAL CO.,LTD.
Labeler DUNS
557795909
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-14
Public Version
2
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
1140acea-8e9d-4c8e-b745-e03a02bbd39b

Device Description

Rod Pre-Bent 6.0 x 90mm

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
MR Unsafe
Direct Marking Exempt
Yes
PM Exempt
No
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
NKB Thoracolumbosacral pedicle screw system
MNH Orthosis, spondylolisthesis spinal fixation
MNI Orthosis, spinal pedicle fixation

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 08800039826358

Customer Contacts

Phone
+82313699470 ext. 112

Premarket Submissions

Submission Number Supplement Number
K122229 000