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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
Dental drill bit extension FDA UDI
Device Name
DRILL SURGAIRTOME TYPE *NO HOSE OR BUR GUARD* DRIVEN BY NITROGEN OR AIR FDA UDI
Model / Reference
00320145 FDA UDI
Description
DRILL SURGAIRTOME TYPE *NO HOSE OR BUR GUARD* DRIVEN BY NITROGEN OR AIR FDA UDI

Identifiers

Catalog Number
00320145 FDA UDI
Primary DI / UDI-DI
00614950010202 FDA UDI
FDA Product Code
DZA FDA UDI
GMDN Term
Dental drill bit extension FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4130 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 — 155 Millimeter FDA UDI

Category: Dental drill bit extension

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

Similar devices

Also classified as Dental drill bit extension.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 62b97ef4-5aa4-4569-8c6e-34a499fe7c57 37 fields · synced May 30, 2026