FDA UDI In Commercial Distribution 🇺🇸 United States

PRIME

DI: 00192629280472 · Model: P3SBMC52 · Microport Orthopedics Inc.
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PRIME
Primary DI
00192629280472
Version / Model
P3SBMC52
Catalog Number
P3SBMC52
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-20
Public Version
1
Public Version Date
2021-09-28
Public Version Status
New
Public Device Record Key
bbd5e061-a1d1-418c-8e01-c9a443fc634e

Device Description

PRIME BIOFOAM MULTI-HOLE SHELL 52 MM GROUP C

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
MR Conditional
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
Yes
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
60516 Metallic acetabulum prosthesis

Identifiers

Type ID
Secondary M684P3SBMC521
Primary 00192629280472

Customer Contacts