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Autofuse Tubing

FDA UDI

Class I (US FDA UDI)

by Mentor Texas LP

Identity

Trade Name
Autofuse Tubing FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
Autofuse Tubing FDA UDI
Model / Reference
AFTU-DS FDA UDI
Description
Autofuse Tubing FDA UDI

Identifiers

Catalog Number
AFTU-DS FDA UDI
Primary DI / UDI-DI
00081317023432 FDA UDI
FDA Product Code
KGZ FDA UDI
GMDN Term
Surgical irrigation/aspiration tubing set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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: Surgical irrigation/aspiration tubing set

Autofuse Tubing by Mentor Texas LP — 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
Mentor Texas LP

Sources (1)

  • FDA UDI 2d6683dd-31ab-4970-9711-f46fd137337f 35 fields · synced Jun 8, 2026