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Aero-Med

FDA UDI

Class I (US FDA UDI)

by Aero-Med Llc

Identity

Trade Name
Aero-Med FDA UDI
Generic Name
General surgical procedure kit, medicated FDA UDI
Device Name
Adhesive Skin Sample Collection Kit FDA UDI
Model / Reference
DT-05250-5 FDA UDI
Description
Adhesive Skin Sample Collection Kit FDA UDI

Identifiers

Catalog Number
DT-05250-5 FDA UDI
Primary DI / UDI-DI
10810010892017 FDA UDI
FDA Product Code
LRP FDA UDI
GMDN Term
General surgical procedure kit, medicated 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

No

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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General surgical procedure kit, medicated

Aero-Med by Aero-Med Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General surgical procedure kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aero-Med Llc

Sources (1)

  • FDA UDI 8d7ad428-0188-45b4-a5dd-e9ccce437fdf 34 fields · synced May 31, 2026