Identity
- Trade Name
- ELECTRACHROME Factor VIII FDA UDI
- Generic Name
- Coagulation factor VIII IVD, kit, chromogenic FDA UDI
- Device Name
- ELECTRACHROME Factor VIII FDA UDI
- Model / Reference
- 049730503 FDA UDI
- Description
- ELECTRACHROME Factor VIII FDA UDI
Identifiers
- Catalog Number
- 049730503 FDA UDI
- Primary DI / UDI-DI
- 08426950101697 FDA UDI
- 510(k) Number
- K981038 FDA UDI
- FDA Product Code
- GGP FDA UDI
- GMDN Term
- Coagulation factor VIII IVD, kit, chromogenic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.7290 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
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Coagulation factor VIII IVD, kit, chromogenic
ELECTRACHROME Factor VIII by Instrumentation Laboratory Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K981038 also covers:
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 II | Pending data |
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Manufacturer
- Manufacturer
- Instrumentation Laboratory Company
Sources (1)
- FDA UDI 692d5ac0-9ce6-4628-b3d7-94035ce45000 37 fields · synced Jun 8, 2026