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NeoChild

FDA UDI

Class I (US FDA UDI)

by Neochild, Llc

Identity

Trade Name
NeoChild FDA UDI
Generic Name
Intravenous administration tubing extension set FDA UDI
Device Name
Umbilical Forceps, 3.5" FDA UDI
Model / Reference
NeoChild FDA UDI
Description
Umbilical Forceps, 3.5" FDA UDI

Identifiers

Catalog Number
NC200002 FDA UDI
Primary DI / UDI-DI
00108163360204 FDA UDI
FDA Product Code
KDD FDA UDI
GMDN Term
Intravenous administration tubing extension set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Intravenous administration tubing extension set

NeoChild by Neochild, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous administration tubing extension set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neochild, Llc

Sources (1)

  • FDA UDI 1c4a116c-50d6-45f5-b8ee-e9b31316434d 34 fields · synced Jun 8, 2026