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Lf

FDA UDI

Class II (US FDA UDI)

by Liebel-Flarsheim Company, LLC

Identity

Trade Name
LF FDA UDI
Generic Name
Radiographic procedure tubing FDA UDI
Device Name
Tubing with Male Luer Adapter (High Pressure) FDA UDI
Model / Reference
601280 FDA UDI
Description
Tubing with Male Luer Adapter (High Pressure) FDA UDI

Identifiers

Primary DI / UDI-DI
10746190002086 FDA UDI
510(k) Number
K882329 FDA UDI
FDA Product Code
DXT FDA UDI
GMDN Term
Radiographic procedure tubing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 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

Yes

FDA UDI

Dimensions & Sizes

Size
Pressure — 6895 KiloPascal FDA UDI
Pressure — 1000 Pound per Square Inch FDA UDI
Length — 76 Centimeter FDA UDI
Length — 30 Inch FDA UDI

Category: Radiographic procedure tubing

Lf by Liebel-Flarsheim Company, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiographic procedure tubing.

Cleared under the same submission

K882329 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6db7ae24-6e3e-4fce-8cbb-9f26e8addd38 35 fields · synced May 30, 2026