← Back to catalogue

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
General specimen container IVD, no additive, sterile FDA UDI
Device Name
SPECIMEN CONTAINER, STERILE, 4 OZ. EA. FDA UDI
Model / Reference
SEA01 FDA UDI
Description
SPECIMEN CONTAINER, STERILE, 4 OZ. EA. FDA UDI

Identifiers

Catalog Number
SEA01 FDA UDI
Primary DI / UDI-DI
00812460028360 FDA UDI
FDA Product Code
FMH FDA UDI
GMDN Term
General specimen container IVD, no additive, sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 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

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: General specimen container IVD, no additive, sterile

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 General specimen container IVD, no additive, sterile.

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 c042b3c9-3fd3-4be9-a9cf-b6f8ec87858e 36 fields · synced May 30, 2026