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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
Oxygen administration tubing FDA UDI
Device Name
6' N2O DISS TO DISS FEMALE NITROUS OXIDE ASSY. BLUE DISS FEMALE TO DISS FEMALE FDA UDI
Model / Reference
5231221 FDA UDI
Description
6' N2O DISS TO DISS FEMALE NITROUS OXIDE ASSY. BLUE DISS FEMALE TO DISS FEMALE FDA UDI

Identifiers

Catalog Number
5231221 FDA UDI
Primary DI / UDI-DI
00614950025329 FDA UDI
FDA Product Code
GDR FDA UDI
GMDN Term
Oxygen administration tubing 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 6 Feet FDA UDI

Category: Oxygen administration tubing

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

Similar devices

Also classified as Oxygen administration tubing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cf726a8d-47f6-46ab-ab95-b6e382cc5656 37 fields · synced May 30, 2026