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ROBINSON HEALTHCARE LIMITED

US

Last updated May 27, 2026

Part of Robinson Healthcare Ltd

What ROBINSON HEALTHCARE LIMITED makes

Robinson Healthcare Limited manufactures single-use surgical instruments, including soft-tissue manipulation forceps, scissors, and tweezers, as well as vaginal speculums and general surgical scissors. The company also produces non-medicated suture kits and obstetrical/gynaecological procedure kits.

The company's products are regulated as Class I and Class II devices and are listed in the FDA UDI database. Robinson Healthcare Limited is based in the United States.

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

Frequently asked questions

What does Robinson Healthcare Limited make?

Robinson Healthcare Limited manufactures single-use surgical instruments such as soft-tissue manipulation forceps, scissors, tweezers, vaginal speculums, and general surgical scissors. The company also produces non-medicated suture kits and obstetrical/gynaecological procedure kits, as stated in the device data summary.

Where is Robinson Healthcare Limited based?

Robinson Healthcare Limited is based in the United States, as explicitly stated in the summary section of the device data provided.

Which regulatory registries list Robinson Healthcare Limited's devices?

Robinson Healthcare Limited's devices are listed in the FDA UDI database, as indicated in the LISTED IN field of the device data. This is the only registry mentioned in the provided information.

How are Robinson Healthcare Limited's devices classified?

Robinson Healthcare Limited's devices are regulated as Class I and Class II devices, as specified in the DEVICE CLASSES field of the device data. Classification is based on risk, with Class I being lowest risk and Class II requiring special controls.

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

Information

Country
US
Address
—
Website
mdpps-inc.com
LinkedIn
—
Facebook
—
Phone
858 4871859
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
237799775

Catalogue (406)

Page 1 of 9
DeviceModel / ReferenceRegistriesClassStatus
Instrapac 8867
FDA UDI
Class IActive
Instrapac 8248
FDA UDI
Class IActive
Instrapac 8120
FDA UDI
Class IActive
Instrapac 8299
FDA UDI
Class IActive
Instrapac 8863
FDA UDI
Class IActive
Instrapac 8118
FDA UDI
Class IActive
Instrapac 7134
FDA UDI
Class IActive
Instrapac 8514
FDA UDI
Class IActive
Instrapac 8158
FDA UDI
Class IActive
Instrapac 8111
FDA UDI
Class IActive
Instrapac 7899
FDA UDI
Class IActive
Instraspec 8870
FDA UDI
Class IIActive
Instrapac 7395
FDA UDI
Class IActive
Instrapac 7964
FDA UDI
Class IActive
Instrapac 7808
FDA UDI
Class IActive
Instrapac 8255
FDA UDI
Class IActive
Instrapac 8187
FDA UDI
Class IIActive
Instrapac 8263
FDA UDI
Class IActive
Instrapac 8802
FDA UDI
Class IActive
Instrapac 8243
FDA UDI
Class IActive
Instrapac 7939
FDA UDI
Class IActive
Instrapac 8192
FDA UDI
Class IActive
Instraspec 8102 Vaginal Speculum Medium-Long
FDA UDI
Class IIActive
Instrapac 7033
FDA UDI
Class IActive
Instrapac 7141
FDA UDI
Class IActive
Instrapac 7084
FDA UDI
Class IActive
Instrapac 7989
FDA UDI
Class IActive
Instrapac 7053
FDA UDI
Class IActive
Instrapac 7967
FDA UDI
Class IActive
Instrapac 8578
FDA UDI
Class IActive
Instrapac 7809
FDA UDI
Class IActive
Instrapac 8293
FDA UDI
Class IActive
Instrapac 8279
FDA UDI
Class IActive
Ultraspec 9149
FDA UDI
Class IIActive
Instrapac 8503
FDA UDI
Class IActive
Instrapac 7026
FDA UDI
Class IActive
Instrapac 7846
FDA UDI
Class IActive
Instrapac 7972
FDA UDI
Class IActive
Instrapac 7982
FDA UDI
Class IActive
Instrapac 8834
FDA UDI
Class IActive
Instrapac 7095
FDA UDI
Class IActive
Instrapac 8086
FDA UDI
Class IActive
Instrapac 7917
FDA UDI
Class IActive
Instrapac 8780
FDA UDI
Class IActive
Instrapac 8264
FDA UDI
Class IActive
Ultraspec 9142
FDA UDI
Class IIActive
Instrapac 8191
FDA UDI
Class IActive
Instrapac 7886
FDA UDI
Class IActive
Instrapac 8848
FDA UDI
Class IActive
Instrapac 7023
FDA UDI
Class IActive

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