Identity
- Trade Name
- Regard™ FDA UDI
- Generic Name
- Fluid/device delivery cardiac catheter FDA UDI
- Device Name
- SPECIAL PROCEDURE FDA UDI
- Model / Reference
- HT00253H FDA UDI
- Description
- SPECIAL PROCEDURE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10194717115144 FDA UDI
- FDA Product Code
- OES FDA UDI
- GMDN Term
- Fluid/device delivery cardiac catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1200 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Fluid/device delivery cardiac catheter
Regard™ by Roi Cps, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Fluid/device delivery cardiac catheter.
- Bariatric Long-Term Care Bed — Dynarex Corp. · Class II
- Helical Infusion Catheter — Biocardia, Inc. · Class II
- Regard™ — ROI CPS, LLC · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Roi Cps, Llc
Sources (1)
- FDA UDI 19d30aab-2525-49c7-b98a-fa0e0b9a0ef1 33 fields · synced Jun 1, 2026