← Back to catalogue

Capture™

FDA UDI

Class I (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name
CAPTURE™ FDA UDI
Generic Name
Intramedullary canal cleaning brush, reusable FDA UDI
Device Name
CAPTURE™ High Torque Screw System The cannula cleaning stylet is used to clean all cannulated instruments. This instrument is used with 4.0 and 5.0 mm instruments. FDA UDI
Model / Reference
AW-3205 FDA UDI
Description
CAPTURE™ High Torque Screw System The cannula cleaning stylet is used to clean all cannulated instruments. This instrument is used with 4.0 and 5.0 mm instruments. FDA UDI

Identifiers

Catalog Number
AW3205 FDA UDI
Primary DI / UDI-DI
10381780242130 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Intramedullary canal cleaning brush, reusable 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Intramedullary canal cleaning brush, reusable

Capture™ by Ascension Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intramedullary canal cleaning brush, reusable.

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 07c16171-303a-4cbf-89df-9fac1e2be225 37 fields · synced May 30, 2026