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Sign in to claim this brandpro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung
US
Last updated May 23, 2026
What pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung makes
Pro Med Instruments GmbH manufactures reusable surgical instruments and systems for neurosurgical and open surgery procedures. Their product portfolio includes skull clamps, surgical retractor systems and blades, neurosurgical headrests, and bipolar electrosurgical handpieces and electrodes.
The devices are classified as Class I and Class II medical devices and are listed in the FDA's Unique Device Identification (FDA UDI) system. The company 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 Pro Med Instruments GmbH manufacture?
Pro Med Instruments GmbH manufactures reusable surgical instruments and systems for neurosurgical and open surgery procedures, including skull clamps, surgical retractor systems and blades, neurosurgical headrests, and bipolar electrosurgical handpieces and electrodes, as stated in the provided summary.
Where is Pro Med Instruments GmbH based?
Pro Med Instruments GmbH is based in the United States, as explicitly stated in the SUMMARY section of the device data.
Which regulatory registry lists the devices of Pro Med Instruments GmbH?
The devices of Pro Med Instruments GmbH are listed in the FDA's Unique Device Identification (FDA UDI) system, as indicated in the LISTED IN field and confirmed in the SUMMARY.
How are the devices of Pro Med Instruments GmbH classified?
The devices of Pro Med Instruments GmbH are classified as Class I and Class II medical devices, as specified in the DEVICE CLASSES field and reiterated in the SUMMARY.
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
- 313517922
Catalogue (404)
Page 2 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| DORO® ADF NON-STICK Bipolar Forceps | 5043.012 | FDA UDI | Class II | Unknown |
| DORO® ADF NON-STICK Bipolar Forceps | 5045.022 | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5039.055 | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5027.014 | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5004-06 | FDA UDI | Class II | Unknown |
| DORO® Micro Blade | 3116-54 | FDA UDI | Class I | Active |
| DORO® NON-STICK Bipolar Forceps | 5025.024 | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5022.054 | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5034.102TL3 | FDA UDI | Class II | Unknown |
| DORO® ADF NON-STICK Bipolar Forceps | 5045.024 | FDA UDI | Class II | Unknown |
| DORO® Quick-Clamp | 1201.010 | FDA UDI | Class II | Active |
| DORO® Sterilization Tray | 5015-50 | FDA UDI | Class II | Active |
| DORO® NON-STICK Bipolar Forceps | 5025.025 | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5023.017 | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5007-02 | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5034.092TL3 | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5032.062TL3 | FDA UDI | Class II | Unknown |
| DORO® Blade | 3116-60 | FDA UDI | Class I | Active |
| DORO® Micro Blade | 3116-20 | FDA UDI | Class I | Active |
| DORO® Blade | 3116-102 | FDA UDI | Class I | Active |
| DORO® NON-STICK Bipolar Forceps | 5022.059TL3B | FDA UDI | Class II | Unknown |
| DORO® Adaptor | 3114-64 | FDA UDI | Class II | Active |
| DORO® Reusable Bipolar Cable | 5015-11 | FDA UDI | Class II | Unknown |
| DORO® Blade | 3116-123 | FDA UDI | Class I | Active |
| DORO® NON-STICK Bipolar Forceps | 5061.053 | FDA UDI | Class II | Unknown |
| DORO LUCENT® iMRI Transfer Collision Indicator | 4003.133 | FDA UDI | Class II | Active |
| DORO® Blade | 3116-601 | FDA UDI | Class I | Active |
| DORO® ADF NON-STICK Bipolar Forceps | 5045.013 | FDA UDI | Class II | Unknown |
| DORO® ADF NON-STICK Bipolar Forceps | 5043.022 | FDA UDI | Class II | Unknown |
| DORO® Micro Blade | 3116-52 | FDA UDI | Class I | Active |
| DORO® ADF NON-STICK Bipolar Forceps | 5044.024 | FDA UDI | Class II | Unknown |
| DORO® Sterile Disposable Skull Pins | 3006-00 | FDA UDI | Class II | Active |
| DORO® NON-STICK Bipolar Forceps | 5022.019TL3B | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5027.017 | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5032.013 | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5022.012TL9 | FDA UDI | Class II | Unknown |
| DORO® Skull Clamp | 1001.010 | FDA UDI | Class II | Active |
| DORO® NON-STICK Bipolar Forceps | 5024.063 | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5023.026 | FDA UDI | Class II | Unknown |
| DORO® Retractor Sterilization Tray | 1201.093 | FDA UDI | Class II | Active |
| DORO® Skull Clamp | 3020-50 | FDA UDI | Class II | Active |
| DORO LUNA® Retractor System | 1203.200 | FDA UDI | Class II | Active |
| DORO® Base Unit | 3001-012 | FDA UDI | Class II | Active |
| DORO® Micro Blade | 3116-22 | EUDAMEDFDA UDI | Class I | Active |
| DORO® NON-STICK Bipolar Forceps | 5027.013 | FDA UDI | Class II | Unknown |
| DORO® ADF NON-STICK Bipolar Forceps | 5043.014 | FDA UDI | Class II | Unknown |
| DORO® NON-STICK Bipolar Forceps | 5038.012 | FDA UDI | Class II | Unknown |
| DORO® Sterilization Case | 3114-58 | FDA UDI | Class II | Active |
| DORO® ADF NON-STICK Bipolar Forceps | 5059.014 | FDA UDI | Class II | Unknown |
| DORO LUCENT® iMRI Transfer Collision Indicator | 4003.135 | FDA UDI | Class II | Active |
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