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Summit Medical 9mm Nozzle with Nozzle Extruder

FDA UDI

Class I (US FDA UDI)

by Summit Medical, LLC

Identity

Trade Name
Summit Medical 9mm Nozzle with Nozzle Extruder FDA UDI
Generic Name
Orthopaedic cement injection cannula FDA UDI
Device Name
9mm Nozzle with Nozzle Extruder FDA UDI
Model / Reference
N700 FDA UDI
Description
9mm Nozzle with Nozzle Extruder FDA UDI

Identifiers

Primary DI / UDI-DI
15060238200322 FDA UDI
FDA Product Code
KIH FDA UDI
GMDN Term
Orthopaedic cement injection cannula FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4200 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

No

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

Yes

FDA UDI

Category: Orthopaedic cement injection cannula

Summit Medical 9mm Nozzle with Nozzle Extruder by Summit Medical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic cement injection cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Summit Medical, LLC

Sources (1)

  • FDA UDI 3ed65869-13d3-4941-8269-8828be7e2895 34 fields · synced May 30, 2026