FDA UDI In Commercial Distribution 🇺🇸 United States

Prophecy

DI: 00192629403147 · Model: PNV10679 · Microport Orthopedics Inc.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Prophecy
Primary DI
00192629403147
Version / Model
PNV10679
Catalog Number
PNV10679
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-27
Public Version
1
Public Version Date
2023-10-05
Public Version Status
New
Public Device Record Key
31a0d8f1-ae13-4797-afcb-6cef9c2b5374
Distribution End Date
2028-09-27

Device Description

PROPHECY® ALIGNMENT GUIDES

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
MBH PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
60826 Custom-made orthopaedic/craniofacial surgical guide

Identifiers

Type ID
Secondary M684PNV106791
Primary 00192629403147

Customer Contacts