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Intelijet

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
INTELIJET FDA UDI
Generic Name
Rigid endoscopic cannula, single-use FDA UDI
Device Name
CLR-TRC CMP DSP INTLJT CANN 5.5X72 STR FDA UDI
Model / Reference
7209989 FDA UDI
Description
CLR-TRC CMP DSP INTLJT CANN 5.5X72 STR FDA UDI

Identifiers

Catalog Number
7209989 FDA UDI
Primary DI / UDI-DI
03596010510839 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Rigid endoscopic cannula, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 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

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

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: Rigid endoscopic cannula, single-use

Intelijet by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 48525365-2873-4ccd-ac8c-849f1d14a569 35 fields · synced Jun 8, 2026