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Sign in to claim this brandGBUK LTD
US
Last updated May 23, 2026
What GBUK LTD makes
GBUK Ltd manufactures single-use and reusable patient handling devices, including transfer sheets, airway suction catheters, mobile lifting system seats, and general-purpose lifting slings/harnesses. Their portfolio also includes inflatable sliding mattresses for patient transfers and patient lifting stretchers designed for clinical mobility support.
The company’s devices are classified under FDA regulations as Class I and Class II, with all products listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to applicable U.S. medical device compliance requirements.
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 Ltd manufacture?
GBUK Ltd specializes in patient handling and mobility devices. Their product range includes single-use and reusable items like patient transfer sheets, airway suction catheters, mobile lifting system seats, general-purpose lifting slings/harnesses, inflatable sliding mattresses for transfers, and patient lifting stretchers. These devices are designed to support clinical mobility and safe patient movement in healthcare settings.
Where is GBUK Ltd based, and what does that mean for their regulatory compliance?
GBUK Ltd is based in the United States. As a U.S.-based manufacturer, their devices must comply with FDA regulations, including classification under FDA’s medical device categories. The company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and regulatory transparency.
How are GBUK Ltd’s devices classified under FDA regulations?
GBUK Ltd’s devices fall under two FDA classification tiers: Class I and Class II. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. The classification depends on the specific device type and its intended use.
Are GBUK Ltd’s devices listed in any regulatory registries?
Yes, GBUK Ltd’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system assigns a unique product identifier to each device, enabling better tracking, transparency, and compliance with FDA requirements. This helps healthcare providers and regulators verify device details and ensure proper use.
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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- 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
- 738810980
Catalogue (83)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Banana | B-EGF140200P | FDA UDI | Class I | Active |
| TenderTip | TT03-14-T34-N | FDA UDI | Class I | Active |
| Banana | PATPAQ-EGF140200 | FDA UDI | Class I | Active |
| Banana | B-SOLOSLIDE200075 | FDA UDI | Class I | Active |
| Banana | DGF100220H | FDA UDI | Class I | Active |
| Banana | DGF100100 | FDA UDI | Class I | Active |
| Banana | B-VERSAL-WH | FDA UDI | Class I | Active |
| Banana | NWF85190H | FDA UDI | N/A | Active |
| Banana | DGT200140 | FDA UDI | Class I | Active |
| Banana | EGT100120 | FDA UDI | Class I | Active |
| TenderTip | TT02-14-T34-N | FDA UDI | Class I | Active |
| Banana | DGT100150 | FDA UDI | Class I | Active |
| Banana | EGF120200 | FDA UDI | Class I | Active |
| TenderTip | TT02-07-P31 | FDA UDI | Class I | Active |
| Banana | EGF100220H | FDA UDI | Class I | Active |
| Banana | B-EGT100200-P | EUDAMEDFDA UDI | Class I | Active |
| Banana | LGT055120 | FDA UDI | Class I | Active |
| Banana | DGF100220 | FDA UDI | Class I | Active |
| Banana | B-DGF072200P | FDA UDI | Class I | Active |
| TenderTip | TT02-12-T34-N | FDA UDI | Class I | Active |
| TenderTip | TT02-07-E31 | FDA UDI | Class I | Active |
| Banana | LGT090200 | FDA UDI | Class I | Active |
| Banana | B-DGF140200P | FDA UDI | Class I | Active |
| TenderTip | TT02-14-E54-N | FDA UDI | Class I | Active |
| Banana | DGF072200 | FDA UDI | Class I | Active |
| Banana | DGT100230 | FDA UDI | Class I | Active |
| Banana | DGF100150 | FDA UDI | Class I | Active |
| Banana | B-DGF100200P | FDA UDI | Class I | Active |
| Banana | B-VERSAL-SPUH | FDA UDI | Class I | Active |
| Banana | PATPAQ-DGF140200/H | FDA UDI | Class I | Active |
| Banana | B-SSPUL-XL | FDA UDI | Class I | Active |
| TenderTip | TT03-14-E54-N | FDA UDI | Class I | Active |
| Banana | B-DG-REDI100200FT | FDA UDI | Class I | Active |
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