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Equinoxe

FDA UDI

Class II (US FDA UDI)

by Exactech, Inc.

Identity

Trade Name
Equinoxe FDA UDI
Generic Name
Orthopaedic instrument extractor FDA UDI
Device Name
HUMERAL STEM EXTRACTOR FDA UDI
Model / Reference
301-09-11 FDA UDI
Description
HUMERAL STEM EXTRACTOR FDA UDI

Identifiers

Catalog Number
301-09-11 FDA UDI
Primary DI / UDI-DI
10885862557698 FDA UDI
510(k) Number
K042021 FDA UDI
K061454 FDA UDI
FDA Product Code
HSD FDA UDI
KWS FDA UDI
GMDN Term
Orthopaedic instrument extractor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
888.3660 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 instrument extractor

Equinoxe by Exactech, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic instrument extractor.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Exactech, Inc.

Sources (1)

  • FDA UDI 38a11a5e-e286-4d6e-a0a0-71be21c7b4db 35 fields · synced May 30, 2026