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BENCOX Total Hip System

FDA UDI

Class II (US FDA UDI)

by Corentec Co., Ltd

Identity

Trade Name
BENCOX Total Hip System FDA UDI
Generic Name
Non-constrained polyethylene acetabular liner FDA UDI
Device Name
BENCOX Mirabo PE Liner - Elevated type 10° 28/42mm FDA UDI
Model / Reference
H1.L67.2842 FDA UDI
Description
BENCOX Mirabo PE Liner - Elevated type 10° 28/42mm FDA UDI

Identifiers

Primary DI / UDI-DI
08800068901521 FDA UDI
510(k) Number
K220468 FDA UDI
FDA Product Code
LPH FDA UDI
LZO FDA UDI
GMDN Term
Non-constrained polyethylene acetabular liner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3353 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-constrained polyethylene acetabular liner

BENCOX Total Hip System by Corentec Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-constrained polyethylene acetabular liner.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corentec Co., Ltd

Sources (1)

  • FDA UDI 4d3add26-5fd5-4508-88fe-92c74c1ce19b 35 fields · synced May 30, 2026