Identity
- Trade Name
- Ritter FDA UDI
- Generic Name
- Chair/stool armrest FDA UDI
- Device Name
- The Ritter 230 adjustable arm system is designed to offer patients a stable platform in accessing the table and sense of security during positioning. Arms rotate and lock into one of three possible positions and are removable, all without the use of tools. FDA UDI
- Model / Reference
- 9A328001 FDA UDI
- Description
- The Ritter 230 adjustable arm system is designed to offer patients a stable platform in accessing the table and sense of security during positioning. Arms rotate and lock into one of three possible positions and are removable, all without the use of tools. FDA UDI
Identifiers
- Catalog Number
- 9A328001 FDA UDI
- Primary DI / UDI-DI
- 00841709111037 FDA UDI
- FDA Product Code
- GBB FDA UDI
- GMDN Term
- Chair/stool armrest FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4960 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: Chair/stool armrest
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 4dfb789b-757b-4f82-b74a-11e9bd7e8b5d 35 fields · synced Jun 8, 2026