← Back to catalogue

SunMed

FDA UDI

Class I (US FDA UDI)

by SunMed

Identity

Trade Name
SunMed FDA UDI
Generic Name
Laryngoscope blade, single-use FDA UDI
Device Name
ALL METAL F/O DISP PHILLIPS SZ 1 FDA UDI
Model / Reference
5-5339-01 FDA UDI
Description
ALL METAL F/O DISP PHILLIPS SZ 1 FDA UDI

Identifiers

Catalog Number
5-5339-01 FDA UDI
Primary DI / UDI-DI
10889483165935 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Laryngoscope blade, 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

Dimensions & Sizes

Size
Length — 113 Millimeter FDA UDI

Category: Laryngoscope blade, single-use

SunMed by SunMed — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope blade, single-use.

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
SunMed

Sources (1)

  • FDA UDI 756b31f1-9b97-4e0d-81b2-8fab1dc87e58 36 fields · synced May 31, 2026