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Basnws -30/150

FDA UDI

Class II (US FDA UDI)

by Pathen Medical Llc

Identity

Trade Name
BASNWS -30/150 FDA UDI
Generic Name
Peripheral vascular/subcutaneous catheter FDA UDI
Device Name
Administration Set, NO Spike, 150 Micron Filter, 30cc Syringe FDA UDI
Model / Reference
BASNWS -30/150 FDA UDI
Description
Administration Set, NO Spike, 150 Micron Filter, 30cc Syringe FDA UDI

Identifiers

Primary DI / UDI-DI
00850005864561 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Peripheral vascular/subcutaneous catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

No

FDA UDI

Category: Peripheral vascular/subcutaneous catheter

Basnws -30/150 by Pathen Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular/subcutaneous catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pathen Medical Llc

Sources (1)

  • FDA UDI df80c115-5361-4b37-9257-a43ecc63212e 34 fields · synced Jun 1, 2026