Identity
- Trade Name
- CRYOcheck™ Platelet Lysate FDA UDI
- Generic Name
- Lupus anticoagulant marker IVD, reagent FDA UDI
- Model / Reference
- PNP-10 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00843876000435 FDA UDI
- 510(k) Number
- K982062 FDA UDI
- FDA Product Code
- GGW FDA UDI
- GMDN Term
- Lupus anticoagulant marker IVD, reagent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.7925 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Lupus anticoagulant marker IVD, reagent
CRYOcheck™ Platelet Lysate by Precision Biologic — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Lupus anticoagulant marker IVD, reagent.
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- LA 1 Screening Reagent — SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Class I
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- LA 2 Confirmation Reagent — SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Class I
- CRYOcheck™ LA Check™ — Precision Biologic · Class I
- CRYOcheck™ LA Check™ — Precision Biologic · Class I
- CRYOcheck™ LA Sure™ — Precision Biologic · Class I
- CRYOcheck™ LA Check™ — Precision Biologic · Class I
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
- Precision Biologic
Sources (1)
- FDA UDI c4f4320e-eac7-4c05-836e-c7a30fd387ff 33 fields · synced May 30, 2026