Identity
- Trade Name
- IMMY FDA UDI
- Generic Name
- Histoplasma capsulatum antigen IVD, control FDA UDI
- Device Name
- Histoplasma Galactomannan Negative Control FDA UDI
- Model / Reference
- HGMNC1 FDA UDI
- Description
- Histoplasma Galactomannan Negative Control FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00816387020445 FDA UDI
- FDA Product Code
- OHQ FDA UDI
- GMDN Term
- Histoplasma capsulatum antigen IVD, control FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1660 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
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Histoplasma capsulatum antigen IVD, control
Immy by Immuno-Mycologics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Histoplasma capsulatum antigen IVD, control.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Immuno-Mycologics, Inc.
Sources (1)
- FDA UDI 7f901b01-1a31-4cc3-b516-9cf357e5d07a 34 fields · synced May 31, 2026