Identity
- Trade Name
- INTERCEPT Blood System FDA UDI
- Generic Name
- Pathogen inactivation/reduction system FDA UDI
- Device Name
- INTERCEPT INT100 Illuminator FDA UDI
- Model / Reference
- INT100 FDA UDI
- Description
- INTERCEPT INT100 Illuminator FDA UDI
Identifiers
- Primary DI / UDI-DI
- 18717953196948 FDA UDI
- FDA Product Code
- PJF FDA UDI
- GMDN Term
- Pathogen inactivation/reduction system FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Pathogen inactivation/reduction system
INTERCEPT Blood System by Cerus Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 III | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Cerus Corporation
Sources (1)
- FDA UDI 09f5bb28-8431-424b-9f6d-fb00d664b576 34 fields · synced May 30, 2026