FDA UDI In Commercial Distribution 🇺🇸 United States

VISIONAIRE

DI: 00885556492673 · Model: V0100083 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VISIONAIRE
Primary DI
00885556492673
Version / Model
V0100083
Catalog Number
V0100083
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-28
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
dc2b4ffb-adea-4554-bdfc-6b9568208833

Device Description

VISIONAIRE JOURNEY II CUTTING BLOCK KIT- RIGHT

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
47815 Orthopaedic implant aiming/guiding block, reusable

Identifiers

Type ID
Primary 00885556492673

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K082358 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 0