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Skytron

FDA UDI

Class II (US FDA UDI)

by Skytron, LLC

Identity

Trade Name
Skytron FDA UDI
Generic Name
Suction/irrigation tubing, single-use FDA UDI
Device Name
Adapter tubing 7/8x3/8x2 FDA UDI
Model / Reference
SkyVac FDA UDI
Description
Adapter tubing 7/8x3/8x2 FDA UDI

Identifiers

Catalog Number
SES6 FDA UDI
Primary DI / UDI-DI
10841736100803 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Suction/irrigation tubing, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2 Inch FDA UDI
Outer Diameter — 0.375 Inch FDA UDI
Outer Diameter — 0.875 Inch FDA UDI

Category: Suction/irrigation tubing, single-use

Skytron by Skytron, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation tubing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Skytron, LLC

Sources (1)

  • FDA UDI 348f2c20-eb81-4671-b196-59440112891d 36 fields · synced May 30, 2026