Tissue-Tek®
O.C.T. Compound
1manufacturer
1catalogue number
Who Else Makes It
Registered in Jiangsu.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Diatrust Medical Co., Ltd. | Nanjing | Jiangsu | Manufacturer | 48 |
Record
| Listed by | Sakura Finetek U.S.A., Inc., United States |
|---|---|
| FDA product code | KEQ |
| Device type | Media, Mounting, Water Soluble |
| Device class | Class 1 |
| Regulation | 21 CFR 864.4010 |
| Establishment | Specification developer, Complaint-file establishment, Manufacturer |
| Premarket notification | Exempt |
| Record published | 2019-12-15 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Label carries | lot or batch number, expiry date, manufacturing date |
| UDI direct marking | Exempt |
Catalogue Numbers
| Catalogue number | Size | Per pack | Status |
|---|---|---|---|
| 4583 | 12 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Epredia | Richard-Allan Scientific LLC | 15 |
| Leica Biosystems | Leica Biosystems Richmond, Inc. | 3 |
| Fisherbrand | Fisher Scientific Company L.L.C. | 1 |
| Media, Mounting, Water Soluble | Scientific Device Laboratory, Inc. | 1 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.