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Djo Surgical

FDA UDI

Class III (US FDA UDI)

by Encore Medical, L.p.

Identity

Trade Name
DJO SURGICAL FDA UDI
Generic Name
Non-constrained polyethylene acetabular liner FDA UDI
Device Name
Replacement HXL Liner 28mm / 10 Degree Hooded - Size 52/54 FDA UDI
Model / Reference
496-28-152 FDA UDI
Description
Replacement HXL Liner 28mm / 10 Degree Hooded - Size 52/54 FDA UDI

Identifiers

Primary DI / UDI-DI
00888912087216 FDA UDI
FDA Product Code
MRA FDA UDI
GMDN Term
Non-constrained polyethylene acetabular liner FDA UDI

Classification

Device Class
Class III 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

Djo Surgical by Encore Medical, L.p. — Class III — 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

Sources (1)

  • FDA UDI 22dfb86a-f48e-448e-b3c3-9d55d318c4b0 34 fields · synced Jun 8, 2026