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Aveta Auto 5 Fr Disposable Resecting Device

FDA UDI

Class II (US FDA UDI)

by Meditrina, Inc.

Identity

Trade Name
Aveta Auto 5 Fr Disposable Resecting Device FDA UDI
Generic Name
Tissue morcellation system handpiece, line-powered FDA UDI
Device Name
Aveta Auto 5 Fr Disposable Resecting Device for use with Aveta System FDA UDI
Model / Reference
215-2023 FDA UDI
Description
Aveta Auto 5 Fr Disposable Resecting Device for use with Aveta System FDA UDI

Identifiers

Catalog Number
215-2023 FDA UDI
Primary DI / UDI-DI
00850006759668 FDA UDI
FDA Product Code
HIG FDA UDI
HIH FDA UDI
FAJ FDA UDI
GMDN Term
Tissue morcellation system handpiece, line-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1700 FDA UDI
884.1690 FDA UDI
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tissue morcellation system handpiece, line-powered

Aveta Auto 5 Fr Disposable Resecting Device by Meditrina, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue morcellation system handpiece, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Meditrina, Inc.

Sources (1)

  • FDA UDI ae8e0c19-4c84-481d-ab35-7ee76ecf22fc 34 fields · synced Jun 1, 2026