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NOVADAQ®and PINPOINT®

FDA UDI

Class II (US FDA UDI)

by Novadaq Technologies Inc

Identity

Trade Name
NOVADAQ®and PINPOINT® FDA UDI
Generic Name
Gastrointestinal endoscopic insufflator FDA UDI
Model / Reference
PP9063 FDA UDI

Identifiers

Primary DI / UDI-DI
00858701006308 FDA UDI
FDA Product Code
HIF FDA UDI
GMDN Term
Gastrointestinal endoscopic insufflator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1730 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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Gastrointestinal endoscopic insufflator

NOVADAQ®and PINPOINT® by Novadaq Technologies Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastrointestinal endoscopic insufflator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0134fa3f-24cd-4e39-a0e8-7e21422d6d01 32 fields · synced May 30, 2026