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Nc602000

FDA UDI

Class II (US FDA UDI)

by Neochild, Llc

Identity

Trade Name
NC602000 FDA UDI
Generic Name
Syringe-loaded medication/vaccine injector, manual, professional FDA UDI
Device Name
Enteral Only 20ml Syringe with Oral Cap FDA UDI
Model / Reference
NC602000 FDA UDI
Description
Enteral Only 20ml Syringe with Oral Cap FDA UDI

Identifiers

Primary DI / UDI-DI
10816336022091 FDA UDI
510(k) Number
K103830 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
Syringe-loaded medication/vaccine injector, manual, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Syringe-loaded medication/vaccine injector, manual, professional

Nc602000 by Neochild, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Syringe-loaded medication/vaccine injector, manual, professional.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neochild, Llc

Sources (1)

  • FDA UDI 4072595c-9818-4f08-a76a-ab3c00f5962e 35 fields · synced Jun 8, 2026