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Ohmega R

FDA UDI

Class II (US FDA UDI)

by Medical Measurement Systems B.V.

Identity

Trade Name
Ohmega R FDA UDI
Generic Name
Oesophageal motility analysis system FDA UDI
Model / Reference
G2-1 FDA UDI

Identifiers

Primary DI / UDI-DI
08717775955016 FDA UDI
FDA Product Code
FFX FDA UDI
GMDN Term
Oesophageal motility analysis system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1725 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Oesophageal motility analysis system

Ohmega R by Medical Measurement Systems B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oesophageal motility analysis system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Measurement Systems B.V.

Sources (1)

  • FDA UDI 5fd134a6-8c54-40d5-b455-cfb1a06142a9 32 fields · synced May 30, 2026