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b-ONE™ Primary Acetabular System

FDA UDI

Class II (US FDA UDI)

by b-ONE Ortho Corp.

Identity

Trade Name
b-ONE™ Primary Acetabular System FDA UDI
Generic Name
Non-constrained polyethylene acetabular liner FDA UDI
Device Name
Acetabular Liner, Neutral, 0 degree; Vitamin E UHMWPE; 32mm Inner Diameter, Size G FDA UDI
Model / Reference
881200321G FDA UDI
Description
Acetabular Liner, Neutral, 0 degree; Vitamin E UHMWPE; 32mm Inner Diameter, Size G FDA UDI

Identifiers

Catalog Number
881200321G FDA UDI
Primary DI / UDI-DI
00843575102287 FDA UDI
FDA Product Code
MEH FDA UDI
HWC FDA UDI
LZO FDA UDI
GMDN Term
Non-constrained polyethylene acetabular liner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3040 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

b-ONE™ Primary Acetabular System by b-ONE Ortho Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-constrained polyethylene acetabular liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
b-ONE Ortho Corp.

Sources (1)

  • FDA UDI 97693236-4cd7-4316-afb0-5f231593f460 34 fields · synced Jun 1, 2026