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Conserve®

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
CONSERVE® FDA UDI
Generic Name
Femoral head/stem prosthesis adaptor FDA UDI
Device Name
CONSERVE® TOTAL MEDIUM NECK SLEEVE FDA UDI
Model / Reference
38NS0000 FDA UDI
Description
CONSERVE® TOTAL MEDIUM NECK SLEEVE FDA UDI

Identifiers

Catalog Number
38NS0000 FDA UDI
Primary DI / UDI-DI
M68438NS00001 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
Femoral head/stem prosthesis adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Femoral head/stem prosthesis adaptor

Conserve® by MicroPort Orthopedics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femoral head/stem prosthesis adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a921e1aa-b622-4908-9b84-80b6bb305d3c 35 fields · synced Jun 9, 2026