← Back to catalogue

C-Mac

FDA UDI

Class I (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
C-MAC FDA UDI
Generic Name
Rigid non-bladed intubation laryngoscope, video FDA UDI
Device Name
C-MAC Video Laryngoscope D-BLADE, Ped. FDA UDI
Model / Reference
8403HXP FDA UDI
Description
C-MAC Video Laryngoscope D-BLADE, Ped. FDA UDI

Identifiers

Primary DI / UDI-DI
04048551389423 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Rigid non-bladed intubation laryngoscope, video FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5540 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Rigid non-bladed intubation laryngoscope, video

C-Mac by Karl Storz GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid non-bladed intubation laryngoscope, video.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Karl Storz GmbH & Co. KG

Sources (1)

  • FDA UDI 741e81e6-eaf9-4dfb-8192-c3ffdd14aea9 33 fields · synced Jun 1, 2026