← Back to catalogue

Ace

FDA UDI

Class I (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
ACE FDA UDI
Generic Name
Orthopaedic implant driver FDA UDI
Device Name
5.0MM TRICAM HAND SQUARE DRIVER TOOL LONG BLUE SS 17-4(H900) FDA UDI
Model / Reference
20156902 FDA UDI
Description
5.0MM TRICAM HAND SQUARE DRIVER TOOL LONG BLUE SS 17-4(H900) FDA UDI

Identifiers

Catalog Number
20156902 FDA UDI
Primary DI / UDI-DI
00614950009954 FDA UDI
FDA Product Code
HWR FDA UDI
GMDN Term
Orthopaedic implant driver FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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 — 14 Millimeter FDA UDI

Category: Orthopaedic implant driver

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

Similar devices

Also classified as Orthopaedic implant driver.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e98020e0-10d6-46fa-a98a-47f7c5ed736a 37 fields · synced May 31, 2026