← Back to catalogue

Dealmed

FDA UDI

Class I (US FDA UDI)

by Dealmed Medical Supplies Llc

Identity

Trade Name
Dealmed FDA UDI
Generic Name
Tongue depressor, examination, single-use FDA UDI
Device Name
Tongue Depressor Sterile Wood 5 1/2" Junior 1's, 100/Bx FDA UDI
Model / Reference
782023 FDA UDI
Description
Tongue Depressor Sterile Wood 5 1/2" Junior 1's, 100/Bx FDA UDI

Identifiers

Catalog Number
782023 FDA UDI
Primary DI / UDI-DI
00817415020192 FDA UDI
FDA Product Code
FMA FDA UDI
GMDN Term
Tongue depressor, examination, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6230 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tongue depressor, examination, single-use

Dealmed by Dealmed Medical Supplies Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tongue depressor, examination, 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

Sources (1)

  • FDA UDI afc20107-ed52-44cc-8aae-ece5ba8651d0 35 fields · synced May 30, 2026