FDA UDI Not in Commercial Distribution 🇺🇸 United States

RBK Patello Femoral

DI: 09340499004655 · Model: GO-1003-36-00 · GLOBAL MANUFACTURING TECHNOLOGY PTY LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RBK Patello Femoral
Primary DI
09340499004655
Version / Model
GO-1003-36-00
Catalog Number
GO-1003-36-00
Company Name
GLOBAL MANUFACTURING TECHNOLOGY PTY LIMITED
Labeler DUNS
752039982
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-07
Public Version
5
Public Version Date
2021-07-14
Public Version Status
Update
Public Device Record Key
2d616ce9-093a-4825-81b2-ba5be9e3d399
Distribution End Date
2021-07-14

Device Description

RBK Patella 36mm

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
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
KRR Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer

GMDN Terms

Code Name
34199 Polyethylene patella prosthesis

Identifiers

Type ID
Primary 09340499004655

Customer Contacts

Phone
+6128870100

Premarket Submissions

Submission Number Supplement Number
K050473 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 36 mm