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GBUK ENTERAL LIMITED

US

Last updated May 23, 2026

What GBUK ENTERAL LIMITED makes

GBUK Enteral Limited manufactures enteral feeding and drainage products, including nasogastric feeding tubes, single-use oral/enteral syringes with ENFit connectors, and gastric drainage bags. Their portfolio also covers protective caps and vial adaptors for enteral nutrition, as well as pH strips for gastric monitoring and stoma buttons for intestinal or urinary applications. Extension sets for enteral tubes are also part of their product range.

These devices are regulated under FDA pathways, with most classified as Class I or Class II, and are listed under the 510(k) and UDI programs. The company operates from the United States, adhering to applicable medical device regulations for enteral and drainage products.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does GBUK Enteral Limited manufacture?

GBUK Enteral Limited specializes in enteral feeding and drainage devices. Their product range includes nasogastric feeding tubes, single-use oral/enteral syringes with ENFit connectors, gastric drainage/decompression bags, and protective caps for enteral tubes. They also produce vial/bottle adaptors, gastric pH strips for monitoring, and stoma buttons for intestinal or urinary applications. These devices are designed to support enteral nutrition and gastrointestinal decompression.

Where is GBUK Enteral Limited based, and what regulations do their devices follow?

GBUK Enteral Limited is based in the United States. Their devices are regulated under FDA pathways, including the 510(k) premarket notification process and the Unique Device Identifier (UDI) system. Since most of their products fall under Class I or Class II classifications, they must comply with FDA requirements for enteral and drainage devices, ensuring safety, performance, and proper labeling.

Which regulatory registries or databases list GBUK Enteral Limited’s devices?

GBUK Enteral Limited’s devices are listed under the FDA’s 510(k) premarket clearance program and the UDI system. These registries ensure traceability and compliance tracking for medical devices in the U.S. The 510(k) process verifies that a device is at least as safe and effective as a legally marketed predicate device, while the UDI system provides a unique identifier for each device to improve tracking and reduce medical errors.

How are GBUK Enteral Limited’s devices classified under FDA regulations?

GBUK Enteral Limited’s devices are primarily classified as Class I or Class II under FDA regulations. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional performance standards or special controls due to moderate risk. The classification depends on factors like the device’s intended use, potential risks, and the body system it interacts with, such as enteral feeding or gastric drainage.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
216643186

Catalogue (191)

Page 1 of 4
DeviceModel / ReferenceRegistriesClassStatus
Enteral EISO-60BNS-US
FDA UDI
Class IIActive
Nutricare YNC08.110ISOSAF-ROW
FDA UDI
Class IIActive
Enteral VED-692
FDA UDI
Class IActive
Enteral SEISO-PFC-12
FDA UDI
Class IIActive
Enteral CT60
FDA UDI
Class IActive
Enteral VED-690
FDA UDI
Class IActive
Enteral VED-670
FDA UDI
Class IActive
Enteral NCC-08-75
FDA UDI
Class IIActive
Nutricare NCF06.60
FDA UDI
Class IIActive
Enteral EN-PLUG-S
FDA UDI
Class IActive
Enteral FNISO-38
FDA UDI
Class IActive
Enteral ELDISO-PFC-6
FDA UDI
Class IIActive
Enteral ECISO-10
FDA UDI
Class IIActive
Nutricare YNC06.110ISOSAF-ROW
FDA UDI
Class IIActive
Enteral EISO-100
FDA UDI
Class IIUnknown
Nutricare YNC08.110ISOSAF-ROW
FDA UDI
Class IIActive
Enteral ABELDISO-PFCO-3
FDA UDI
Class IIActive
Enteral SELDISO-PFC-3
FDA UDI
Class IIActive
Enteral ESCF.075-ISOSAF-US
FDA UDI
Class IIActive
Enteral PFC-100
FDA UDI
Class IActive
Enteral ENT-PHSPPX
FDA UDI
Class IActive
CareTip ABOSPFCO-20-200NS
FDA UDI
Class IActive
Nutricare NCF06.50
FDA UDI
Class IIActive
Enteral NCC-04-75
FDA UDI
Class IIActive
Enteral NC08.080ISOSAF-ROW
FDA UDI
Class IIActive
CareTip OS-1
FDA UDI
Class IActive
Enteral NCF05.90
FDA UDI
Class IIActive
Enteral EISO-PFC-12
FDA UDI
Class IIActive
Nutricare YNC08.050ISOSAF-ROW
FDA UDI
Class IIActive
Nutricare NCF05.60
FDA UDI
Class IIActive
Nutricare YNC06.080ISOSAF-ROW
FDA UDI
Class IIActive
Enteral ELDISO-1
FDA UDI
Class IIUnknown
Nutricare NCF04.50
FDA UDI
Class IIActive
Enteral SEISO-PFC-35
FDA UDI
Class IIActive
Enteral NCF06.50
FDA UDI
Class IIActive
Enteral NCF10.110
FDA UDI
Class IIActive
Enteral EISO-35BNS-US
FDA UDI
Class IIUnknown
Enteral ELDISO-2.5
FDA UDI
Class IIUnknown
Enteral NCF06.75
FDA UDI
Class IIActive
Nutricare YNC10.092ISOSAF-ROW
FDA UDI
Class IIActive
Enteral NCC-05-50
FDA UDI
Class IIActive
Enteral EISO-20BNS-US
FDA UDI
Class IIActive
Enteral MSISO-150P
FDA UDI
Class IActive
CareTip ABOSPFCO-10-500NS
FDA UDI
Class IActive
Enteral MSISO-100P
FDA UDI
Class IActive
Enteral ENT-PHX
FDA UDI
Class IActive
Enteral EISONN-10
FDA UDI
Class IIUnknown
Enteral VED-693
FDA UDI
Class IActive
Enteral ABELDISO-PFCO-1
FDA UDI
Class IIActive
Kentec AMP-PIBA-2
FDA UDI
Class IActive

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