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Gastric Alimetry Array

FDA UDI

Class II (US FDA UDI)

by Alimetry , Ltd.

Identity

Trade Name
Gastric Alimetry Array FDA UDI
Generic Name
Myoelectric gastrointestinal motility analysis system FDA UDI
Device Name
Gastric Alimetry Array FDA UDI
Model / Reference
AS001-1 FDA UDI
Description
Gastric Alimetry Array FDA UDI

Identifiers

Primary DI / UDI-DI
09421906857016 FDA UDI
FDA Product Code
MYE FDA UDI
GMDN Term
Myoelectric gastrointestinal motility analysis system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1735 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Myoelectric gastrointestinal motility analysis system

Gastric Alimetry Array by Alimetry , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Myoelectric gastrointestinal motility analysis system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alimetry , Ltd.

Sources (1)

  • FDA UDI e1f5ca0c-b015-4abf-98f9-0a2dd4c56ae9 35 fields · synced May 30, 2026