FDA UDI In Commercial Distribution 🇺🇸 United States

BENCOX THR System

DI: 08800068949301 · Model: HA.01K.4048 · Corentec Co., Ltd
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BENCOX THR System
Primary DI
08800068949301
Version / Model
HA.01K.4048
Company Name
Corentec Co., Ltd
Labeler DUNS
688739895
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-20
Public Version
1
Public Version Date
2021-07-28
Public Version Status
New
Public Device Record Key
6524ec74-bfde-4ad5-83b2-59eee8898f4e

Device Description

Bencox Mirabo PE Liner Trial 40E-STD-PPX

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
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

GMDN Terms

Code Name
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 08800068949301

Customer Contacts

Phone
+82415857114

Premarket Submissions

Submission Number Supplement Number
K211866 000