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Hermes

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
HERMES FDA UDI
Generic Name
Insufflation gas conditioning system control unit FDA UDI
Device Name
INTERFACE KIT HERMES TO S&N 400 INSUF FDA UDI
Model / Reference
7210017 FDA UDI
Description
INTERFACE KIT HERMES TO S&N 400 INSUF FDA UDI

Identifiers

Catalog Number
7210017 FDA UDI
Primary DI / UDI-DI
03596010493736 FDA UDI
510(k) Number
K050580 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Insufflation gas conditioning system control unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Insufflation gas conditioning system control unit

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

Similar devices

Also classified as Insufflation gas conditioning system control unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI e8016712-a5bf-43b7-9653-e013a27a27ee 36 fields · synced Jun 8, 2026