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EarClear Rx

FDA UDI

Class I (US FDA UDI)

by Nuance Medical, Llc

Identity

Trade Name
EarClear Rx FDA UDI
Generic Name
Tissue specimen microdissection system mechanical excision tip IVD FDA UDI
Device Name
EarClear Rx Disposable Tips- 3 pack FDA UDI
Model / Reference
90007 FDA UDI
Description
EarClear Rx Disposable Tips- 3 pack FDA UDI

Identifiers

Catalog Number
90007 FDA UDI
Primary DI / UDI-DI
00856331006224 FDA UDI
FDA Product Code
KCP FDA UDI
GMDN Term
Tissue specimen microdissection system mechanical excision tip IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.5220 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tissue specimen microdissection system mechanical excision tip IVD

EarClear Rx by Nuance Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue specimen microdissection system mechanical excision tip IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nuance Medical, Llc

Sources (1)

  • FDA UDI cd7313f0-717d-46a3-b092-015923b07a7f 35 fields · synced May 30, 2026