FDA UDI In Commercial Distribution 🇺🇸 United States

Bencox Hip System

DI: 08800017287058 · Model: HA.08E.0004 · Corentec Co., Ltd
Product Codes
3
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bencox Hip System
Primary DI
08800017287058
Version / Model
HA.08E.0004
Company Name
Corentec Co., Ltd
Labeler DUNS
688739895
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-20
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
f86f1129-e007-4479-8453-75c802484a19

Device Description

Bencox M Stem Modular Rasp #4

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

GMDN Terms

Code Name
58481 Femoral stem prosthesis trial
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 08800017287058

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K152084 000
K162127 000