← Back to catalogue

Spy Paq

FDA UDI

Class II (US FDA UDI)

by Novadaq Technologies Inc

Identity

Trade Name
SPY PAQ FDA UDI
Generic Name
General surgical procedure kit, medicated FDA UDI
Model / Reference
LC3006 FDA UDI

Identifiers

Catalog Number
LC3006 FDA UDI
Primary DI / UDI-DI
10858701006268 FDA UDI
510(k) Number
K182907 FDA UDI
FDA Product Code
IZI FDA UDI
GMDN Term
General surgical procedure kit, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1600 FDA UDI
Commercial Distribution
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

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: General surgical procedure kit, medicated

Spy Paq by Novadaq Technologies Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General surgical procedure kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 91a85d7c-ac70-41a6-9bea-e3f66d008bf8 36 fields · synced May 30, 2026