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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
Carbide dental bur, reusable FDA UDI
Device Name
BUR BONE CUTTER 44MM 4HD 9CL STRYKER NOTCH FDA UDI
Model / Reference
31440020S FDA UDI
Description
BUR BONE CUTTER 44MM 4HD 9CL STRYKER NOTCH FDA UDI

Identifiers

Catalog Number
31440020S FDA UDI
Primary DI / UDI-DI
00614950012282 FDA UDI
FDA Product Code
EJL FDA UDI
GMDN Term
Carbide dental bur, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3240 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

No

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
Outer Diameter — 2.3 Millimeter FDA UDI

Category: Carbide dental bur, reusable

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

Similar devices

Also classified as Carbide dental bur, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 050ba588-2cf1-42ae-8b69-b7061b4fdf8b 37 fields · synced May 30, 2026