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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
Staple Removal Kit Sterile, Ea FDA UDI
Model / Reference
784022 FDA UDI
Description
Staple Removal Kit Sterile, Ea FDA UDI

Identifiers

Catalog Number
784022 FDA UDI
Primary DI / UDI-DI
00817415020499 FDA UDI
FDA Product Code
MCZ FDA UDI
GMDN Term
Tongue depressor, examination, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

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: 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

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Manufacturer

Sources (1)

  • FDA UDI 14f61722-d7e3-4254-a571-984f55d49ed0 34 fields · synced May 31, 2026