Capture™

FDA UDI

Class I (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name: CAPTURE™ FDA UDI
Generic Name: Cannulated surgical drill bit, single-use FDA UDI
Device Name: CAPTURE™ High Torque Screw System The tap is a tool used to produce a threaded hole. FDA UDI
Model / Reference: CNT-5000-511-050 FDA UDI
Description: CAPTURE™ High Torque Screw System The tap is a tool used to produce a threaded hole. FDA UDI

Identifiers

Catalog Number: NT5000511050 FDA UDI
Primary DI / UDI-DI: 10381780242901 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Cannulated surgical drill bit, single-use 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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Cannulated surgical drill bit, single-use

Capture™ by Ascension Orthopedics, 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: Ascension Orthopedics, Inc.

Sources (1)

FDA UDI ec184d92-4dab-4019-889d-5fb73ea7da58 37 fields · synced Jun 1, 2026