FDA UDI In Commercial Distribution 🇺🇸 United States

PROCOTYL® PRIME

DI: M684P3LFTB221 · Model: P3LFTB22 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PROCOTYL® PRIME
Primary DI
M684P3LFTB221
Version / Model
P3LFTB22
Catalog Number
P3LFTB22
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-30
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
b10843f6-1718-479e-b3ea-190ef4ad16f5

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
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
HWT TEMPLATE

GMDN Terms

Code Name
44742 Joint prosthesis implantation kit, reusable

Identifiers

Type ID
Primary M684P3LFTB221

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 22 Millimeter