FDA UDI In Commercial Distribution 🇺🇸 United States

Revision Knee System

DI: 00840286843218 · Model: 2977-1-0004 · Shalby Advanced Technologies, Inc.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Revision Knee System
Primary DI
00840286843218
Version / Model
2977-1-0004
Catalog Number
2977-1-0004
Company Name
Shalby Advanced Technologies, Inc.
Labeler DUNS
085976260
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-22
Public Version
1
Public Version Date
2025-05-30
Public Version Status
New
Public Device Record Key
9893c0bc-10e6-4c48-8f39-d1a51d513cfd

Device Description

RKS, Sizer, Tibial Baseplate, Left, Size 4

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
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
HWT Template

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable
46479 Surgical implant template, reusable

Identifiers

Type ID
Primary 00840286843218

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Sizer, Tibial Baseplate, Left, Size 4