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SunMed

FDA UDI

Class I (US FDA UDI)

by SunMed

Identity

Trade Name
SunMed FDA UDI
Generic Name
Endotracheal tube holder FDA UDI
Device Name
ALUMINUM STYLET 16" ADULT PK/10 FDA UDI
Model / Reference
9-0204-10 FDA UDI
Description
ALUMINUM STYLET 16" ADULT PK/10 FDA UDI

Identifiers

Catalog Number
9-0204-10 FDA UDI
Primary DI / UDI-DI
10889483007082 FDA UDI
FDA Product Code
BSR FDA UDI
GMDN Term
Endotracheal tube holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5790 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endotracheal tube holder

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

Similar devices

Also classified as Endotracheal tube holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SunMed

Sources (1)

  • FDA UDI 69a3b436-9ea8-4660-b1aa-92b9599ef3bf 35 fields · synced May 30, 2026