Ace

FDA UDI

Class I (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name: ACE FDA UDI
Generic Name: Intravenous line recessed-needle connector FDA UDI
Device Name: CATHETER ONLY 14G 2" NS TEFLON PLAS HUB 10/PKG L/F FDA UDI
Model / Reference: 0039940 FDA UDI
Description: CATHETER ONLY 14G 2" NS TEFLON PLAS HUB 10/PKG L/F FDA UDI

Identifiers

Catalog Number: 0039940 FDA UDI
Primary DI / UDI-DI: 00614950017072 FDA UDI
FDA Product Code: GCB FDA UDI
GMDN Term: Intravenous line recessed-needle connector FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 2 Inch FDA UDI

Category: Intravenous line recessed-needle connector

Ace by Ace Surgical Supply Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Ace Surgical Supply Co., Inc.

Sources (1)

FDA UDI b05f19d3-8bd5-48bf-9343-5eeb8d2435c3 37 fields · synced May 30, 2026