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Cathtong Ii

FDA UDI

Class II (US FDA UDI)

by L & Z Us, Inc.

Identity

Trade Name
CATHTONG II FDA UDI
Generic Name
Peripherally-inserted central venous catheter FDA UDI
Device Name
5F Dual Lumen PICC Kit FDA UDI
Model / Reference
5252111 FDA UDI
Description
5F Dual Lumen PICC Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00861744000134 FDA UDI
510(k) Number
K170486 FDA UDI
K232594 FDA UDI
FDA Product Code
LJS FDA UDI
GMDN Term
Peripherally-inserted central venous catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5970 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Dimensions & Sizes

Size
Catheter Gauge — 5 French FDA UDI
Length — 55 Centimeter FDA UDI

Category: Peripherally-inserted central venous catheter

Cathtong Ii by L & Z Us, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripherally-inserted central venous catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
L & Z Us, Inc.

Sources (1)

  • FDA UDI b398430e-c1b2-4aca-b6f4-a723e67c9332 36 fields · synced Jun 8, 2026