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Luna Paq®

FDA UDI

by Novadaq Technologies Inc

Identity

Trade Name
LUNA PAQ® FDA UDI
Generic Name
General surgical procedure kit, medicated FDA UDI
Model / Reference
LU3001 FDA UDI

Identifiers

Primary DI / UDI-DI
10858701006244 FDA UDI
GMDN Term
General surgical procedure kit, medicated FDA UDI

Classification

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

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

Category: General surgical procedure kit, medicated

Luna Paq® by Novadaq Technologies Inc — 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

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Manufacturer

Sources (1)

  • FDA UDI 9da9af73-afbc-4576-8c9b-d982f78a64a5 32 fields · synced Jun 8, 2026