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Sign in to claim this brandMYCO MEDICAL SUPPLIES INC.
US
Last updated May 23, 2026
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 879187821
Catalogue (731)
Page 1 of 15| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Reli® | SHN18G101-S1ML-LDS | FDA UDI | Class II | Active |
| Reli® | V340-M | FDA UDI | Class II | Active |
| Reli | PT556-P | FDA UDI | Class II | Active |
| Reli | GC636-P | FDA UDI | Class II | Active |
| Reli | P8695-P | FDA UDI | Class II | Active |
| Reli | N1663-P | FDA UDI | Class II | Active |
| Reli | INSY30G18751-S1ML | FDA UDI | Class II | Active |
| Wealy® RELI® | SS10ML22G151 | FDA UDI | Class II | Active |
| Reli® | GSIS21G-3 | FDA UDI | Class II | Active |
| Reli® | SHN21G151-S10ML | FDA UDI | Class II | Active |
| Reli | GP821-BRC | FDA UDI | Class II | Active |
| Reli® | GC203-M | FDA UDI | Class II | Active |
| Reli | SHN24G151 | FDA UDI | Class II | Active |
| Reli | SHN25G6251 | FDA UDI | Class II | Active |
| Wealy® RELI® | SS5ML23G101 | FDA UDI | Class II | Active |
| Reli | VU494-P | FDA UDI | Class II | Active |
| Reli | R-FSC1820B | FDA UDI | Class II | Active |
| Reli® | SHN23G101-S3ML-LDS | FDA UDI | Class II | Active |
| Reli® | ML333-M | FDA UDI | Class II | Active |
| Reli® | ML398-M | FDA UDI | Class II | Active |
| Reli® | HYP20G101-RW-S5ML | FDA UDI | Class II | Active |
| Reli | SHN27G051 | FDA UDI | Class II | Active |
| Reli® | P8683-M | FDA UDI | Class II | Active |
| Reli® | SBCN-R20G101T | FDA UDI | Class II | Active |
| Reli® | GP324-M | FDA UDI | Class II | Active |
| Reli® | V339-M | FDA UDI | Class II | Active |
| Reli® | SBCN-R22G114T | FDA UDI | Class II | Active |
| Reli® | SBCN-R21G101T | FDA UDI | Class II | Active |
| Reli® | N661-M | FDA UDI | Class II | Active |
| Reli | N661-P | FDA UDI | Class II | Active |
| Myco | 6001-3M | FDA UDI | Class I | Active |
| Reli | SHN30G051-S1ML-LDS | FDA UDI | Class II | Active |
| Reli | MS316-SI | FDA UDI | Class II | Active |
| Reli | BCN-R21G101 | FDA UDI | Class II | Active |
| Reli | SHN23G151 | FDA UDI | Class II | Active |
| Reli® | P1013-M | FDA UDI | Class II | Active |
| Reli® | GSBCS25G-7 | FDA UDI | Class II | Active |
| Reli | S10ML-BFN18G151 | FDA UDI | Class II | Active |
| Reli | BCN-R20G101 | FDA UDI | Class II | Active |
| Reli | N668-SI | FDA UDI | Class II | Active |
| Reli® | SHN21G101-S5ML | FDA UDI | Class II | Active |
| Reli® | GC621-M | FDA UDI | Class II | Active |
| Reli® | P8684-M | FDA UDI | Class II | Active |
| Reli® | GSBCS23G-7T | FDA UDI | Class II | Active |
| Reli | CHE20G701 | FDA UDI | Class II | Active |
| Myco | 6001-06 | FDA UDI | Class I | Active |
| Reli® | SHN20G201 | FDA UDI | Class II | Active |
| Reli | R-CLT1411 | FDA UDI | Class II | Active |
| Reli® | P8687-M | FDA UDI | Class II | Active |
| Reli | V463-SI | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (2)
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 |
|---|---|---|---|---|
| Nov 6, 2015 | Z-0444-2016 | — | terminated | Particulates: Complaints of rubber coring from the closure of injection vials. |
| Feb 7, 2013 | Z-0891-2013 | — | terminated | Pouch labeling/printing errors and defective packaging resulting in possible compromised sterility. |