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Corrugated Tube

FDA UDI

Class I (US FDA UDI)

by Parker Hannifin Corp.

Identity

Trade Name
CORRUGATED TUBE FDA UDI
Generic Name
Vacuum hose FDA UDI
Device Name
CORRUGATED TUBE FDA UDI
Model / Reference
4200 FDA UDI
Description
CORRUGATED TUBE FDA UDI

Identifiers

Catalog Number
4200 FDA UDI
Primary DI / UDI-DI
00816711022343 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Vacuum hose FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vacuum hose

Corrugated Tube by Parker Hannifin Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vacuum hose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4c093e23-7912-4086-98a1-d2db7d8114dd 34 fields · synced Jun 8, 2026