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CI-55 Anesthesia Holster

FDA UDI

Class I (US FDA UDI)

by Instrumentation Industries, Incorporated

Identity

Trade Name
CI-55 Anesthesia Holster FDA UDI
Generic Name
Medical device service rail clamp FDA UDI
Device Name
The CI-55 Anesthesia Holster is a device used to store and handle soiled laryngoscope blades and suction tips to prevent cross contamination and pathogen transmission in the anesthesia work area during intubation of a patient . The CI-55 Anesthesia Holster allows for safe storage and handling of contaminated items such as laryngoscope blades and suction tips until they can be discarded or sent for re-processing. This device is Single Patient Use. Packaged as non-sterile. FDA UDI
Model / Reference
CI-55 FDA UDI
Description
The CI-55 Anesthesia Holster is a device used to store and handle soiled laryngoscope blades and suction tips to prevent cross contamination and pathogen transmission in the anesthesia work area during intubation of a patient . The CI-55 Anesthesia Holster allows for safe storage and handling of contaminated items such as laryngoscope blades and suction tips until they can be discarded or sent for re-processing. This device is Single Patient Use. Packaged as non-sterile. FDA UDI

Identifiers

Catalog Number
CI-55 FDA UDI
Primary DI / UDI-DI
M996CI550 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Medical device service rail clamp 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical device service rail clamp

CI-55 Anesthesia Holster by Instrumentation Industries, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device service rail clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 349cab46-a103-4568-a1ad-2cb8b8fe3296 35 fields · synced Jun 1, 2026