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Smith & Nephew 400

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
SMITH & NEPHEW 400 FDA UDI
Generic Name
Laparoscopic insufflator FDA UDI
Device Name
S&N 400 INSUFFLATOR KIT GERMAN FDA UDI
Model / Reference
7209937 FDA UDI
Description
S&N 400 INSUFFLATOR KIT GERMAN FDA UDI

Identifiers

Catalog Number
7209937 FDA UDI
Primary DI / UDI-DI
03596010542359 FDA UDI
510(k) Number
K022052 FDA UDI
FDA Product Code
HIF FDA UDI
GMDN Term
Laparoscopic 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

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laparoscopic insufflator

Smith & Nephew 400 by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic insufflator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1f047da0-79f3-481e-812c-f0db37d818e3 36 fields · synced Jun 8, 2026