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Aveta Tissue Catch

FDA UDI

Class II (US FDA UDI)

by Meditrina, Inc.

Identity

Trade Name
Aveta Tissue Catch FDA UDI
Generic Name
Surgical tissue/fluid collection bag FDA UDI
Device Name
Aveta Tissue Catch, for use with Aveta System FDA UDI
Model / Reference
205-259 FDA UDI
Description
Aveta Tissue Catch, for use with Aveta System FDA UDI

Identifiers

Catalog Number
205-259 FDA UDI
Primary DI / UDI-DI
00850006759163 FDA UDI
510(k) Number
K190372 FDA UDI
FDA Product Code
HIH FDA UDI
HIG FDA UDI
GMDN Term
Surgical tissue/fluid collection bag FDA UDI

Classification

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

Clinical & Handling

Sterile

No

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: Surgical tissue/fluid collection bag

Aveta Tissue Catch by Meditrina, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical tissue/fluid collection bag.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Meditrina, Inc.

Sources (1)

  • FDA UDI 876f61e5-ad8b-457e-b9ab-10840d466e9f 35 fields · synced Jun 1, 2026