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Rospital Productos Medicos

FDA UDI

Class I (US FDA UDI)

by Atlas Medical Products Llc

Identity

Trade Name
Rospital Productos Medicos FDA UDI
Generic Name
Closed-wound drainage kit FDA UDI
Device Name
CLOSED WOUND DRAINAGE SYSTEM 19 FR, EA. FDA UDI
Model / Reference
AMPCDA06 FDA UDI
Description
CLOSED WOUND DRAINAGE SYSTEM 19 FR, EA. FDA UDI

Identifiers

Catalog Number
AMPCDA06 FDA UDI
Primary DI / UDI-DI
00812460028421 FDA UDI
FDA Product Code
GCY FDA UDI
GMDN Term
Closed-wound drainage kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4680 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Category: Closed-wound drainage kit

Rospital Productos Medicos by Atlas Medical Products Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Closed-wound drainage kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 99423dd8-9180-4cd6-b504-bab5abbdfb5e 36 fields · synced May 30, 2026