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HGPII Acetabular Component

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
HGPII Acetabular Component FDA UDI
Generic Name
Non-constrained polyethylene acetabular liner FDA UDI
Model / Reference
32-6726-02-01 FDA UDI

Identifiers

Catalog Number
32-6726-002-01 FDA UDI
Primary DI / UDI-DI
00889024670259 FDA UDI
510(k) Number
K990135 FDA UDI
FDA Product Code
LPH FDA UDI
GMDN Term
Non-constrained polyethylene acetabular liner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 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

Yes

FDA UDI

Category: Non-constrained polyethylene acetabular liner

HGPII Acetabular Component by Zimmer, Inc. — 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
Zimmer, Inc.

Sources (1)

  • FDA UDI 3510c8c2-ddef-410d-9da2-facb7d37c862 36 fields · synced May 30, 2026