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NeoMagic

FDA UDI

Class II (US FDA UDI)

by Neo Medical Inc.

Identity

Trade Name
NeoMagic FDA UDI
Generic Name
Peripheral intravenous catheterization kit, non-sensing FDA UDI
Device Name
1.9Fr x 6cm Single Lumen Polyurethane EPIV with Stylet & 27ga Sharps Safety Tearaway Sheath Introducer FDA UDI
Model / Reference
1947-1606 FDA UDI
Description
1.9Fr x 6cm Single Lumen Polyurethane EPIV with Stylet & 27ga Sharps Safety Tearaway Sheath Introducer FDA UDI

Identifiers

Catalog Number
1947-1606 FDA UDI
Primary DI / UDI-DI
B339194716060 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Peripheral intravenous catheterization kit, non-sensing 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

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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Catheter Length — 6 Centimeter FDA UDI
Catheter Gauge — 1.9 French FDA UDI
Needle Gauge — 27 Gauge FDA UDI

Category: Peripheral intravenous catheterization kit, non-sensing

NeoMagic by Neo Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral intravenous catheterization kit, non-sensing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neo Medical Inc.

Sources (1)

  • FDA UDI bf9b688d-b659-4ad4-aadb-cc8b00c800cc 37 fields · synced Jun 6, 2026