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Globus (Shetland) Ltd

United Kingdom (ex Northern Ireland) GB-MF-000007384 Last updated 23 May 2026

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Devices
110
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue110

Page 1 of 3

  • Skytec Ref SKG00565IB

    Class I EUDAMED Active

  • Haika Ref HAK8005

    Class I EUDAMED Active

  • Haika Ref HAK8007

    Class I EUDAMED Active

  • Haika Ref HAK0163

    Class I EUDAMED Active

  • Keepsafe Ref BNG00003EF

    Class I EUDAMED Active

  • Haika Ref HAK5101

    Class I EUDAMED Active

  • Haika Ref HAK4505

    Class I EUDAMED Active

  • Haika Ref HAK4503

    Class I EUDAMED Active

  • Keepsafe Ref BNG00002HD

    Class I EUDAMED Active

  • Keepsafe Ref BNG00002HH

    Class I EUDAMED Active

  • Haika Ref HAK4500

    Class I EUDAMED Active

  • Skytec Ref SKG00630BJ

    Class I EUDAMED Active

  • Haika Ref PUR3354

    Class I EUDAMED Active

  • Keepsafe Ref BNG00001DF

    Class I EUDAMED Active

  • Skytec Ref SKG00428DJ

    Class I EUDAMED Active

  • Keepsafe Ref BNG00004CJ

    Class I EUDAMED Active

  • Keepsafe Ref BNG00004CH

    Class I EUDAMED Active

  • Skytec Ref SKG00424DD

    Class I EUDAMED Active

  • Skytec Ref SKG00530EJ

    Class I EUDAMED Active

  • Haika Ref PUR3351

    Class I EUDAMED Active

  • Haika Ref HAK6000

    Class I EUDAMED Active

  • Haika Ref HAK5201

    Class I EUDAMED Active

  • Haika Ref HAK5203

    Class I EUDAMED Active

  • Benchmark Ref BMG00460DH

    Class I EUDAMED Active

  • Skytec Ref SKG00630BF

    Class I EUDAMED Active

  • Skytec Ref SKG00430DJ

    Class I EUDAMED Active

  • Skytec Ref SKG00430DH

    Class I EUDAMED Active

  • Skytec Ref SKG00428DD

    Class I EUDAMED Active

  • Skytec Ref SKG00530ED

    Class I EUDAMED Active

  • Skytec Ref SKG00530EF

    Class I EUDAMED Active

  • Keepsafe Ref BNG00002HJ

    Class I EUDAMED Active

  • Keepsafe Ref BNG00001DJ

    Class I EUDAMED Active

  • Skytec Ref SKYTEAL1

    Class I EUDAMED Active

  • Haika Ref HAK4504

    Class I EUDAMED Active

  • Consumable Solutions Ref 143-5274

    Class I EUDAMED Active

  • Skytec Ref SKG00324IH

    Class I EUDAMED Active

  • Skytec Ref SKG04524EF

    Class I EUDAMED Active

  • Skytec Ref SKG00924BF

    Class I EUDAMED Active

  • Skytec Ref SKG00725GL

    Class I EUDAMED Active

  • Skytec Ref SKYTEAL5

    Class I EUDAMED Active

  • Keepsafe Ref BNG00003EH

    Class I EUDAMED Active

  • Haika Ref HAK0164

    Class I EUDAMED Active

  • Haika Ref HAK4502

    Class I EUDAMED Active

  • Skytec Ref SKG00428DF

    Class I EUDAMED Active

  • Skytec Ref SKG00630BH

    Class I EUDAMED Active

  • Keepsafe Ref BNG00003EJ

    Class I EUDAMED Active

  • Skytec Ref SKYUTAH5

    Class I EUDAMED Active

  • Haika Ref HAK5104

    Class I EUDAMED Active

  • Skytec Ref SKG00724BH

    Class I EUDAMED Active

  • Haika Ref HAK4501

    Class I EUDAMED Active

Showing 1-50 of 110

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FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Globus (Shetland) Limited US

What Globus (Shetland) Ltd makes

Globus (Shetland) Ltd manufactures medical devices including the Keepsafe system, designed for patient positioning and support in clinical settings, and the HAIKA range of surgical drapes and gowns for infection control. The SKYTEC series comprises disposable surgical drapes and gowns, intended for use in sterile procedures to maintain barrier integrity during surgery.

These devices are classified as Class I under EU regulations and are registered in the EUDAMED database. The company operates from the United Kingdom.

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 Globus (Shetland) Ltd manufacture?

Globus (Shetland) Ltd produces a range of medical devices including the Keepsafe system, which is designed for patient positioning and support in clinical environments. They also manufacture the HAIKA range of surgical drapes and gowns, as well as the SKYTEC series of disposable surgical drapes and gowns. These products are intended for use in sterile procedures to ensure patient safety and infection control.

Where is Globus (Shetland) Ltd based?

Globus (Shetland) Ltd is based in the United Kingdom. The company’s headquarters and operations are located there, though specific regional offices or manufacturing sites may vary.

Which regulatory registries list Globus (Shetland) Ltd’s devices?

Globus (Shetland) Ltd’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This platform is used to track and provide transparency on medical devices authorised within the EU market.

How are Globus (Shetland) Ltd’s devices classified under EU regulations?

Globus (Shetland) Ltd’s devices, including the Keepsafe system, HAIKA range, and SKYTEC series, are classified as Class I under EU medical device regulations. This classification applies to low-risk devices that pose minimal risk to patients and users, such as surgical drapes, gowns, and patient positioning aids.

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

Information

Country
United Kingdom (ex Northern Ireland)
Address
T2 Trafford Point, Twining Road, manchester, United Kingdom (ex Northern Ireland)
Phone
+441618774747
PRRC contact
Julien Magniez
EUDAMED SRN
GB-MF-000007384