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: CONNECT HAND DRIVER 4MM SYSTEM 24MM TL SHORT SS 17-4 FDA UDI
Model / Reference: 20953001 FDA UDI
Description: CONNECT HAND DRIVER 4MM SYSTEM 24MM TL SHORT SS 17-4 FDA UDI

Identifiers

Catalog Number: 20953001 FDA UDI
Primary DI / UDI-DI: 00614950010004 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 24 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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Ace Surgical Supply Co., Inc.

Sources (1)

FDA UDI be6870af-380c-4a1f-bf94-314be8a52d1e 37 fields · synced Jun 8, 2026