This page includes the latest FDA filings for Dmb. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3005465238 |
| FEI Number | 3005465238 |
| Name | DMB |
| Owner & Operator | DMB Apparatebau GmbH |
| Contact Address | Spiesheimer Weg 25a Woerrstadt DE-RP Rheinland-Pfalz 55286 DE |
| Official Correspondent |
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| US Agent |
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| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | Spiesheimer Weg 25a Woerrstadt Rheinland-Pfalz, 55286 DE |
| Establishment Type | Sterilize Medical Device for Another Party (Contract Sterilizer) |
Device Company | Device | Date |
|---|---|---|
DMB [DMB Apparatebau GmbH] | SteriVit | 2016-12-06 |
| NCAGE Code | 51M98 | DMB!DBA ADVENTURES IN COLOR |
| CAGE Code | 51M98 | DMB ADVENTURES IN COLOR |
| S.A.M. Registration | 51M98 [787043095] | DMB ADVENTURES IN COLOR |
| DUNS | 787043095 | DMB |
| Import ID | Shipment | Cargo Description | Quantity |
|---|---|---|---|
| 2018012051555 | Gothenburg,Sweden -> New York/Newark Area, Newark, New Jersey | SEALFEX 4025 RG BP, SEAFLEX 4010 TS BP SAMPLE | 14 PKG |