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Elite Medical Instrumentation

FDA UDI

Class I (US FDA UDI)

by Elite Medical Instrumentation

Identity

Trade Name
ELITE MEDICAL INSTRUMENTATION FDA UDI
Generic Name
Extraluminal vascular occluder, reusable FDA UDI
Device Name
Compressor, Conn, Aortic FDA UDI
Model / Reference
EMI-351715 FDA UDI
Description
Compressor, Conn, Aortic FDA UDI

Identifiers

Catalog Number
EMI-351715 COMPRESSOR FDA UDI
Primary DI / UDI-DI
G569EMI3517150 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Extraluminal vascular occluder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Extraluminal vascular occluder, reusable

Elite Medical Instrumentation by Elite Medical Instrumentation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Extraluminal vascular occluder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elite Medical Instrumentation

Sources (1)

  • FDA UDI 68364a3e-f513-4f3c-aedd-2e5d91f5b6ab 34 fields · synced Jun 8, 2026