Identity
- Trade Name
- Ritter FDA UDI
- Generic Name
- Limb/torso/head restraint, reusable FDA UDI
- Device Name
- The Ritter 230 Security Straps are intended to help improve safety by securing the patient to the chair before, during and after procedures, especially when anesthesia is used. The length and location of the straps are both adjustable allowing them to be used for patients of all sizes. FDA UDI
- Model / Reference
- 9A214001 FDA UDI
- Description
- The Ritter 230 Security Straps are intended to help improve safety by securing the patient to the chair before, during and after procedures, especially when anesthesia is used. The length and location of the straps are both adjustable allowing them to be used for patients of all sizes. FDA UDI
Identifiers
- Catalog Number
- 9A214001 FDA UDI
- Primary DI / UDI-DI
- 00841709111082 FDA UDI
- FDA Product Code
- FMQ FDA UDI
- GMDN Term
- Limb/torso/head restraint, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6760 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Limb/torso/head restraint, reusable
Ritter by Midmark Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Midmark Corporation
Sources (1)
- FDA UDI e006ac5a-fdd3-4349-a7b7-9601d735f833 35 fields · synced Jun 8, 2026