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Acetabular Instrument Set

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
Acetabular Instrument Set FDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Device Name
Joint for Ceramic Liner Posititioner FDA UDI
Model / Reference
Joint for Ceramic Liner Positioner FDA UDI
Description
Joint for Ceramic Liner Posititioner FDA UDI

Identifiers

Catalog Number
9058.85.110 FDA UDI
Primary DI / UDI-DI
08033390064569 FDA UDI
FDA Product Code
LPH FDA UDI
MBL FDA UDI
GMDN Term
Orthopaedic inorganic implant inserter/extractor, reusable 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic inorganic implant inserter/extractor, reusable

Acetabular Instrument Set by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic inorganic implant inserter/extractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 67f97d75-73c2-4f50-88f2-2a42e4574954 34 fields · synced Jun 1, 2026