Identity
- Trade Name
- Diazyme FDA UDI
- Generic Name
- Cystatin C IVD, kit, nephelometry/turbidimetry FDA UDI
- Model / Reference
- DZ133C-K FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817089020092 FDA UDI
- GMDN Term
- Cystatin C IVD, kit, nephelometry/turbidimetry FDA UDI
Classification
- 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
No
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: Cystatin C IVD, kit, nephelometry/turbidimetry
Diazyme by Diazyme Laboratories, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Cystatin C IVD, kit, nephelometry/turbidimetry.
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- Tina-quant Cystatin C Gen.2 — Roche Diagnostics Corp. · Class II
- Tina-quant Cystatin C Gen.2 — Roche Diagnostics Corp. · Class II
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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Diazyme Laboratories, Inc.
Sources (1)
- FDA UDI 5edac0d1-975a-4d23-8971-c278166a9eb7 32 fields · synced Jun 9, 2026