2026 CBP ACE & FDA OASIS Enforcement Update: MoCRA Cosmetic FEI & QMSR Device 510(k) Affirmation of Compliance cross-checks are active at Los Angeles, Newark, Miami & Savannah ports.
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OFFICIAL OPENFDA FEI RECORDFEI: 3002806591Reg Yr: 2027Malaysia (MY)

BARD SDN. BHD.

Official US Food and Drug Administration (FDA) Establishment Registration & Device/Facility Listing dossier for BARD SDN. BHD. (FEI 3002806591). Use this record to cross-check CBP ACE Affirmation of Compliance codes (`DEV` / `DFE` / `FEI`), verify the designated US Agent on file, and subscribe to automated Import Alert (DWPE) monitoring.

Registered Facility Address

LOT 57-C, KULIM INDUSTRIAL ESTATE

KULIM Kedah, Malaysia (09000)

FDA FURLS Identifiers

FEI Number: 3002806591

Registration No: 8040607 • Status Code: 1 (Active)

Designated U.S. Agent21 CFR 807.40

Joni Anderson

Franklin Lakes, NJ (USA)

480-2662981

joni.anderson@bd.com

Registered FDA Product Codes, Device Classes & Commercial Names

Cross-check your commercial invoice product descriptions against these active FDA product code filings to prevent NO_510K or UNAPPROVED_NEW_DRUG port holds.

Proprietary / Commercial Brand Names on File

All-Silicone Foley CatheterBardex Silicone Foley Catheter (offered in strips and trays)Lubri-Sil Foley Catheter (offered in strips and trays)Lubri-Sil I.C. Foley Catheter (offered in strips and trays)
Product CodeFDA Classification NameDevice Class21 CFR Regulation510(k) Exempt?
EZLCatheter, Retention Type, BalloonClass 221 CFR 876.5130 Requires 510(k) / Check
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Get an automated Slack/Webhook JSON payload and email alert within 15 minutes whenever FDA OASIS logs a new detention, Import Alert Red List addition, or Warning Letter for BARD SDN. BHD. (FEI 3002806591) before you wire your 70% balance payment.

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Other Verified FDA FEI Establishments in Malaysia

Frequently Asked Questions: FEI 3002806591 (BARD SDN. BHD.)

What is the FDA FEI Number for BARD SDN. BHD.?

According to public US FDA Establishment Registration records, BARD SDN. BHD. (KULIM Kedah, Malaysia) is assigned FDA Facility Establishment Identifier (FEI) 3002806591 (Registration No. 8040607) with registration year 2027.

Who is the designated US Agent for FEI 3002806591 (BARD SDN. BHD.)?

The registered US Agent on file for FEI 3002806591 is Joni Anderson located in Franklin Lakes, NJ. Importers should independently confirm active representation before filing CBP ACE entry.

Does an active FDA FEI registration guarantee that shipments from BARD SDN. BHD. will clear US Customs without detention?

No. An active FDA FEI number or establishment registration only confirms administrative listing in FDA FURLS. Shipments can still be detained at US ports under Detention Without Physical Examination (DWPE / Import Alerts) for labeling, 510(k), cGMP, or adulteration violations.