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Barricaid ACD Extractor

FDA UDI

by Intrinsic Therapeutics

Identity

Trade Name
Barricaid ACD Extractor FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
Reusable extractor designed to facilitate Barricaid ACD removal, should it be necessary. FDA UDI
Model / Reference
400763/400766 FDA UDI
Description
Reusable extractor designed to facilitate Barricaid ACD removal, should it be necessary. FDA UDI

Identifiers

Catalog Number
EXTR-1-A FDA UDI
Primary DI / UDI-DI
M906EXTR1A0 FDA UDI
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Commercial Distribution
Not 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

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

Barricaid ACD Extractor by Intrinsic Therapeutics — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2cc88609-5575-46a6-9f33-ad1809f0be8a 35 fields · synced May 31, 2026