Identity
- Trade Name
- ACU-DTM FDA UDI
- Generic Name
- Multiple dermatophyte species culture isolate identification IVD, kit FDA UDI
- Device Name
- ACU-DTM, Dermatophyte Test Medium, 24/bX FDA UDI
- Model / Reference
- M101 FDA UDI
- Description
- ACU-DTM, Dermatophyte Test Medium, 24/bX FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10814105021214 FDA UDI
- FDA Product Code
- JSJ FDA UDI
- GMDN Term
- Multiple dermatophyte species culture isolate identification IVD, kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.2360 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Multiple dermatophyte species culture isolate identification IVD, kit
Acu-Dtm by Acuderm, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Acuderm, Inc.
Sources (1)
- FDA UDI c2da6409-cb71-4499-93a4-f3b2c940cd09 33 fields · synced Jun 8, 2026