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Ace

FDA UDI

Class I (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
ACE FDA UDI
Generic Name
Stopcock FDA UDI
Device Name
STOPCOCK 3-WAY PLASTIC STERILE DISP L/F 50/BOX FDA UDI
Model / Reference
0031161 FDA UDI
Description
STOPCOCK 3-WAY PLASTIC STERILE DISP L/F 50/BOX FDA UDI

Identifiers

Catalog Number
0031161 FDA UDI
Primary DI / UDI-DI
00614950013456 FDA UDI
FDA Product Code
KGZ FDA UDI
GMDN Term
Stopcock 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Stopcock

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

Similar devices

Also classified as Stopcock.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 049fa989-b27f-40b5-b577-ac1b502eacfe 36 fields · synced May 30, 2026