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Super Bypass

FDA UDI

Class I (US FDA UDI)

by Takayama Instruments Inc.

Identity

Trade Name
Super Bypass FDA UDI
Generic Name
Surgical irrigation/aspiration cannula, non-illuminating, reusable FDA UDI
Device Name
Cleaning Stylet for Tips FDA UDI
Model / Reference
SSTi-028 FDA UDI
Description
Cleaning Stylet for Tips FDA UDI

Identifiers

Catalog Number
SSTi-028 FDA UDI
Primary DI / UDI-DI
04580036674223 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Surgical irrigation/aspiration cannula, non-illuminating, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical irrigation/aspiration cannula, non-illuminating, reusableSurgical irrigation system nozzle

Super Bypass by Takayama Instruments Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation system nozzle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 53a2cf41-c3e1-41c7-9169-16c375f412a9 34 fields · synced May 30, 2026