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Sign in to claim this brandMADA MEDICAL PRODUCTS, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 625 WASHINGTON AVE., CARLSTADT, NJ, 07072
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 2225311
- DUNS Number
- —
Catalogue (185)
Page 3 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Mada Medical Products, Inc. | 401UR | FDA UDI | Class II | Active |
| Mada Medical Products, Inc. | R1835GBHF-25A | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1629DE | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1301BM | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 7000-MVP | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1335 | FDA UDI | Class I | Active |
| Manan Medical Products, Inc. | 502507 | FDA UDI | Class I | Unknown |
| Mada Medical Products, Inc. | 1635-1 | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | R1835-25GB | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1630M-15E | FDA UDI | Class I | Active |
| Mada Medical | 8250 | FDA UDI | Class II | Active |
| Mada Medical Products, Inc. | R1835-25GBMRI | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1443 | FDA UDI | Class I | Active |
| Mada Medical Products | 7021 | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 178B-70 | FDA UDI | Class II | Active |
| Mada Medical Products, Inc. | R1833-15G | FDA UDI | Class I | Active |
| Manan Medical Products, Inc. | 502505 | FDA UDI | Class I | Unknown |
| Mada Medical Products, Inc | 1629 | FDA UDI | Class I | Active |
| Mada Medical Products | 7021 CASE/4 | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1335-1 | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1631 | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1616-AE | FDA UDI | Class I | Active |
| Manan Medical Products, Inc. | 502652 | FDA UDI | Class I | Unknown |
| Mada Medical Products, Inc. | R1836GBHF-25GP | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1411E | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1301ME | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1701-1 | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1301M | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1631E | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 401DEL | FDA UDI | Class II | Active |
| Mada Medical Products, Inc. | R1835-15GE | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1533E | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1528B | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1359 | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1443S-15 | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1335-15 | FDA UDI | Class I | Active |
| Mada Medical Products, Inc. | 1630-15 | FDA UDI | Class I | Active |
| MPM Medical Supply (Private Label) | KOP2003 | FDA UDI | Class I | Active |
| Manan Manta Catheter Fixation Disk | K954132 | FDA 510(k) | Class II | Active |
| Manan Biliary Drainage Catheter | K954043 | FDA 510(k) | Class II | Active |
| Epidural Needle | K980536 | FDA 510(k) | Class II | Active |
| Manan Pro-Mag Automatic Biopsy Device | K914874 | FDA 510(k) | Class II | Active |
| Manan Bio-Cut Soft Tissue Biopsy Needle | K052802 | FDA 510(k) | Class II | Active |
| Manan Adapter For Bip Biopsy Device | K933448 | FDA 510(k) | Class II | Active |
| Manan Adapter For Bard Biopty System | K940365 | FDA 510(k) | Class II | Active |
| Voyage | K930949 | FDA 510(k) | Class II | Active |
| Manan D Bag | K963849 | FDA 510(k) | Class II | Active |
| Manan V.s. Access Needle/Set | K963767 | FDA 510(k) | Class II | Active |
| Simon Breast Lesion Localization Needle | K914941 | FDA 510(k) | Class I | Active |
| Manan Prostate Locking Introducer Set | K961377 | FDA 510(k) | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| May 3, 2005 | Z-0922-05 | — | terminated | The hub of the prostate seeding needle does not release as expected from the applicator as expected during procedures. |