FDA UDI In Commercial Distribution 🇺🇸 United States

PROCOTYL® PRIME

DI: M684P3LESH401 · Model: P3LESH40 · Microport Orthopedics Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
PROCOTYL® PRIME
Primary DI
M684P3LESH401
Version / Model
P3LESH40
Catalog Number
P3LESH40
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-20
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
25be0c8a-eb46-4311-b252-713d1e7b5a5a

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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OQI Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

GMDN Terms

Code Name
43168 Non-constrained polyethylene acetabular liner

Identifiers

Type ID
Primary M684P3LESH401

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 40 Millimeter