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Trabectome Fluidics Set

FDA UDI

Class I (US FDA UDI)

by Neomedix Corp.

Identity

Trade Name
Trabectome Fluidics Set FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
Disposable, single use, surgical Irrigation and Aspiration tubing set FDA UDI
Model / Reference
550034-01 FDA UDI
Description
Disposable, single use, surgical Irrigation and Aspiration tubing set FDA UDI

Identifiers

Primary DI / UDI-DI
00854028002108 FDA UDI
FDA Product Code
KYG FDA UDI
GMDN Term
Surgical irrigation/aspiration tubing set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4360 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

Yes

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 irrigation/aspiration tubing set

Trabectome Fluidics Set by Neomedix Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration tubing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neomedix Corp.

Sources (1)

  • FDA UDI afe00e4c-ff2a-4ccb-97bb-a2b783b9725a 33 fields · synced May 31, 2026