← Back to catalogue

Picc-Nate

FDA UDI

Class II (US FDA UDI)

by Utah Medical Products, Inc.

Identity

Trade Name
PICC-NATE FDA UDI
Generic Name
Peripherally-inserted central venous catheter FDA UDI
Device Name
A Single-Lumen Silicone Peripherally Inserted Central Catheter, 1.9 French FDA UDI
Model / Reference
Catheter FDA UDI
Description
A Single-Lumen Silicone Peripherally Inserted Central Catheter, 1.9 French FDA UDI

Identifiers

Catalog Number
P-2S FDA UDI
Primary DI / UDI-DI
H671P2S0 FDA UDI
510(k) Number
K001874 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

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

No

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 1.9 French FDA UDI

Category: Peripherally-inserted central venous catheter

Picc-Nate by Utah Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripherally-inserted central venous catheter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 8d717a24-063e-45ac-8295-32231137cd59 36 fields · synced Jun 9, 2026