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Nipro Safelet Cath

FDA UDI

Class II (US FDA UDI)

by Nipro Medical Corporation

Identity

Trade Name
NIPRO SAFELET CATH FDA UDI
Generic Name
Peripheral vascular catheter FDA UDI
Device Name
Intravascular catheter FDA UDI
Model / Reference
CI+1650 FDA UDI
Description
Intravascular catheter FDA UDI

Identifiers

Catalog Number
CI+1650-2C FDA UDI
Primary DI / UDI-DI
10383790006313 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Peripheral vascular catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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

Dimensions & Sizes

Size
Needle Gauge — 16 Gauge FDA UDI
Length — 2 Inch FDA UDI

Category: Peripheral vascular catheter

Nipro Safelet Cath by Nipro Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 163a06dc-1b5d-42d2-981c-8fd64a8e0069 36 fields · synced May 30, 2026