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Ameritus

FDA UDI

Class II (US FDA UDI)

by Kentec Medical, Inc.

Identity

Trade Name
Ameritus FDA UDI
Generic Name
ENFit oral/enteral syringe, single-use FDA UDI
Device Name
60ml enteral/oral syringe FDA UDI
Model / Reference
AEG60-KMS FDA UDI
Description
60ml enteral/oral syringe FDA UDI

Identifiers

Catalog Number
AEG60-KMS FDA UDI
Primary DI / UDI-DI
10817522011301 FDA UDI
510(k) Number
K110853 FDA UDI
FDA Product Code
FPD FDA UDI
GMDN Term
ENFit oral/enteral syringe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: ENFit oral/enteral syringe, single-use

Ameritus by Kentec Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENFit oral/enteral syringe, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 40e068a2-3abd-43cf-a939-eca6a18dcdb1 36 fields · synced May 31, 2026