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Barricaid® ACD (Annular Closure Device)

FDA UDI

Class III (US FDA UDI)

by Intrinsic Therapeutics

Identity

Trade Name
Barricaid® ACD (Annular Closure Device) FDA UDI
Generic Name
Intervertebral disc prolapse repair implant FDA UDI
Device Name
Barricaid® Annular Closure Device (ACD), 8mm width/size FDA UDI
Model / Reference
8mm width FDA UDI
Description
Barricaid® Annular Closure Device (ACD), 8mm width/size FDA UDI

Identifiers

Catalog Number
BAR-A8-8MM FDA UDI
Primary DI / UDI-DI
M906BARA88MM0 FDA UDI
PMA Number
P160050 FDA UDI
FDA Product Code
QES FDA UDI
GMDN Term
Intervertebral disc prolapse repair implant FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Intervertebral disc prolapse repair implant

Barricaid® ACD (Annular Closure Device) by Intrinsic Therapeutics — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intervertebral disc prolapse repair implant.

Cleared under the same submission

P160050 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Intrinsic Therapeutics

Sources (1)

  • FDA UDI 90841f30-f7da-4eb4-b3f4-ac71084bad20 37 fields · synced May 29, 2026