Marlen Mfg. & Development Co.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000055888 FEI 1520020
- Devices
- 176
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Catalogue
UltraMax Ref 595225
UltraMax Gemini Ref 20022
UltraMax Gemini Ref 25250
UltraMax Ref 115534
UltraMax Ref 593832
UltraMax Ref 595925
UltraMax Ref 593538
UltraMax Gemini Ref 20019
UltraMax Ref 593744
UltraMax Ref 593529
UltraMax Ref 115244
UltraMax Ref 595244
UltraMax Gemini Ref 20032
UltraMax Ref 593444
UltraMax Ref 595219
UltraMax Ref 593829
UltraMax Ref 595525
UltraMax Gemini Ref 21022
UltraMax Ref 595932
UltraMax Ref 593434
SuperFlat Ref 596112
UltraMax Ref 593125
UltraMax Gemini Ref 20034
UltraMax Ref 593229
UltraMax Gemini Ref 25100
UltraMax Ref 593412
MegaMax Ref 595100
UltraMax Ref 595322
UltraMax Ref 593144
UltraMax Ref 593822
Gemini Belt Ref 29104
UltraMax Ref 595812
UltraMax Ref 115544
UltraMax Ref 593112
Gemini Ref 20000
UltraMax Ref 595222
UltraMax Ref 595329
UltraMax Ref 595338
UltraMax Gemini Ref 21025
UltraMax Ref 593722
UltraMax Ref 593280
MiniMax Ref 53900
UltraMax Ref 595622
UltraMax Ref 595332
UltraMax Ref 595629
UltraMax Ref 595334
UltraMax Ref 593180
UltraMax Ref 595319
UltraMax Ref 593129
SuperFlat Ref 596412
Showing 101-150 of 176
Company details
- EUDAMED SRN
- US-MF-000055888
- FDA FEI number
- 1520020
- EUDAMED status
- Active
- EUDAMED registered name
- Marlen Mfg. & Development Co.
- EUDAMED abbreviated name
- Marlen
- Registered address
- 5150, Richmond Road, 44146, Bedford, United States
- [email protected]
- PRRC contact
- Rik Smits
What Marlen Mfg. & Development Co. makes
Marlen Mfg. & Development Co. manufactures ostomy pouches, including the UltraMax and MARLEN ULTRA ILEOSTOMY POUCH-5000 models.
The company's products are Class I devices and are listed in both the EU's EUDAMED and the FDA's 510(k) registry. Marlen Mfg. & Development Co. is based in the US.