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Kurin Blood Collection Set, 23 Ga, BD Vacutainer
FDA UDIClass II (US FDA UDI)
by Pathway, Llc
Identity
- Trade Name
- Kurin Blood Collection Set, 23 Ga, BD Vacutainer FDA UDI
- Generic Name
- Ultrasound-guided intrauterine radio-frequency ablation system FDA UDI
- Model / Reference
- D-11223 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00851682007043 FDA UDI
- FDA Product Code
- JKA FDA UDI
- GMDN Term
- Ultrasound-guided intrauterine radio-frequency ablation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1675 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Kurin Blood Collection Set, 23 Ga, BD Vacutainer by Pathway, Llc — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Pathway, Llc
Sources (1)
- FDA UDI 5a31cd14-aa7a-4fad-bf2e-250fc3359370 33 fields · synced May 30, 2026