Identity
- Trade Name
- Coda FDA UDI
- Generic Name
- Intravascular occluding balloon catheter, image-guided FDA UDI
- Device Name
- Coda, Balloon Catheter FDA UDI
- Model / Reference
- G53025 FDA UDI
- Description
- Coda, Balloon Catheter FDA UDI
Identifiers
- Catalog Number
- CODA-2-10.0-35-120-40 FDA UDI
- Primary DI / UDI-DI
- 00827002530256 FDA UDI
- FDA Product Code
- DQY FDA UDI
- GMDN Term
- Intravascular occluding balloon catheter, image-guided FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1250 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Intravascular occluding balloon catheter, image-guided
Coda by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intravascular occluding balloon catheter, image-guided.
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- LMI BILUMEN IRRIGATION ARTERIAL EMBOLECTOMY CATHETER — LUCAS MEDICAL INC · Class II
- HyperFormTM — Micro Therapeutics, Inc. · Class II
- CELLO™, Balloon Guide Catheter — Fuji Systems Corp. · 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
- Cook Incorporated
Sources (1)
- FDA UDI e784abb0-0a69-4251-9312-efa8ca2fe69b 36 fields · synced Jun 8, 2026