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Barricaid® ACD Removal Tool

FDA UDI

Class I (US FDA UDI)

by Intrinsic Therapeutics

Identity

Trade Name
Barricaid® ACD Removal Tool FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Single-use disposable tool for removal of the Barricaid® Annular Closure Device (ACD) implant, should it be necessary to do so. FDA UDI
Model / Reference
400921-A FDA UDI
Description
Single-use disposable tool for removal of the Barricaid® Annular Closure Device (ACD) implant, should it be necessary to do so. FDA UDI

Identifiers

Catalog Number
BAR-REMOVAL FDA UDI
Primary DI / UDI-DI
M906BARREMOVAL0 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Category: Orthopaedic surgical procedure kit, non-medicated, reusable

Barricaid® ACD Removal Tool by Intrinsic Therapeutics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Intrinsic Therapeutics

Sources (1)

  • FDA UDI c90da6eb-8479-4863-b66a-bde2824c4c6b 35 fields · synced Jun 1, 2026