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SunMed

FDA UDI

Class I (US FDA UDI)

by SunMed

Identity

Trade Name
SunMed FDA UDI
Generic Name
Laryngoscope handle, single-use FDA UDI
Device Name
Sunmed Disposable Layrngscope handle, stubby, 20/bx, sterile FDA UDI
Model / Reference
5-5338-11 FDA UDI
Description
Sunmed Disposable Layrngscope handle, stubby, 20/bx, sterile FDA UDI

Identifiers

Catalog Number
5-5338-11 FDA UDI
Primary DI / UDI-DI
10889483159033 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Laryngoscope handle, single-use

SunMed by SunMed — 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

Manufacturer
SunMed

Sources (1)

  • FDA UDI be27d6a8-87a7-4b20-ad99-5eb64ffa15d0 35 fields · synced Jun 6, 2026