FDA UDI In Commercial Distribution 🇺🇸 United States

BENCOX Hip System

DI: 08800068900661 · Model: 01.01.486 · Corentec Co., Ltd
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
BENCOX Hip System
Primary DI
08800068900661
Version / Model
01.01.486
Company Name
Corentec Co., Ltd
Labeler DUNS
688739895
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-24
Public Version
1
Public Version Date
2024-06-03
Public Version Status
New
Public Device Record Key
abce3c8b-3249-4b11-9efc-583c4346e603

Device Description

Bencox Delta Option Head 32L

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
No
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
KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

GMDN Terms

Code Name
38156 Ceramic femoral head prosthesis

Identifiers

Type ID
Primary 08800068900661

Premarket Submissions

Submission Number Supplement Number
K223828 000