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Carnegie Surgical LLC

FDA UDI

Class I (US FDA UDI)

by Carnegie Surgical LLC

Identity

Trade Name
Carnegie Surgical LLC FDA UDI
Generic Name
Laryngoscope handle, single-use FDA UDI
Device Name
Laryngoscope green system handle, single use, small (pen light) (requires 2AA batteries, not included), aluminium, with LED lamp (Pack of 10) FDA UDI
Model / Reference
404-5111 FDA UDI
Description
Laryngoscope green system handle, single use, small (pen light) (requires 2AA batteries, not included), aluminium, with LED lamp (Pack of 10) FDA UDI

Identifiers

Catalog Number
404-5111 FDA UDI
Primary DI / UDI-DI
G14140451110 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Laryngoscope handle, single-use 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

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

Yes

FDA UDI

Category: Laryngoscope handle, single-use

Carnegie Surgical LLC by Carnegie Surgical LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope handle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5af20981-da65-4edf-9fd0-7f0286631741 35 fields · synced May 31, 2026