Identity
- Trade Name
- PINPOINT PAQ® FDA UDI
- Generic Name
- Laparoscopic surgical procedure kit, medicated FDA UDI
- Model / Reference
- PP9092 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10858701006220 FDA UDI
- GMDN Term
- Laparoscopic surgical procedure kit, medicated FDA UDI
Classification
- 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
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Pinpoint Paq® by Novadaq Technologies Inc — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Novadaq Technologies Inc
Sources (1)
- FDA UDI 5e2971b4-380d-468c-acc6-6327a8bee371 33 fields · synced May 30, 2026