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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
Surgical drill guide, reusable FDA UDI
Device Name
Two step lag bur 47TL, .8, 1.6 2 Steps HP (SS 17-4 (H900)) FDA UDI
Model / Reference
454282001 FDA UDI
Description
Two step lag bur 47TL, .8, 1.6 2 Steps HP (SS 17-4 (H900)) FDA UDI

Identifiers

Catalog Number
454282001 FDA UDI
Primary DI / UDI-DI
00614950028351 FDA UDI
FDA Product Code
DZA FDA UDI
GMDN Term
Surgical drill guide, reusable 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical drill guide, 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 Surgical drill guide, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 806f9678-2be9-456f-8d95-a2548f03ae3e 35 fields · synced May 30, 2026