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Harmonic

FDA UDI

Class I (US FDA UDI)

by Ethicon Endo-Surgery, Inc.

Identity

Trade Name
Harmonic FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Harmonic Sterilization Tray FDA UDI
Model / Reference
HST01 FDA UDI
Description
Harmonic Sterilization Tray FDA UDI

Identifiers

Catalog Number
HST01 FDA UDI
Primary DI / UDI-DI
20705036012624 FDA UDI
FDA Product Code
LRP FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Harmonic by Ethicon Endo-Surgery, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 60aecb04-fc36-423d-b5cf-e5d83e91f63f 36 fields · synced May 29, 2026