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Sentinel®

FDA UDI

Class II (US FDA UDI)

by Alcor Scientific

Identity

Trade Name
Sentinel® FDA UDI
Generic Name
Enteral feeding pump FDA UDI
Device Name
Sentinel®, Enteral Feeding Pump, 230VAC Type BF FDA UDI
Model / Reference
S-2000-6 FDA UDI
Description
Sentinel®, Enteral Feeding Pump, 230VAC Type BF FDA UDI

Identifiers

Catalog Number
S-2000-6 FDA UDI
Primary DI / UDI-DI
00896406002362 FDA UDI
510(k) Number
K011587 FDA UDI
FDA Product Code
LZH FDA UDI
GMDN Term
Enteral feeding pump FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 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

Yes

FDA UDI

Category: Enteral feeding pump

Sentinel® by Alcor Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Enteral feeding pump.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alcor Scientific

Sources (1)

  • FDA UDI d61570fc-77a0-48c7-8af0-82340c3cda1e 35 fields · synced May 30, 2026