Identity
- Trade Name
- DLP® FDA UDI
- Generic Name
- Coronary sinus cannula FDA UDI
- Device Name
- CANNULA 94735 RCSP SIL AUTO 15FR 10PK FDA UDI
- Model / Reference
- 94735 FDA UDI
- Description
- CANNULA 94735 RCSP SIL AUTO 15FR 10PK FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20643169454754 FDA UDI
- 510(k) Number
- K123762 FDA UDI
- FDA Product Code
- DWF FDA UDI
- GMDN Term
- Coronary sinus cannula FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4210 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
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Catheter Gauge — 15.0 French FDA UDI
Category: Coronary sinus cannula
Dlp® by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Coronary sinus cannula.
- Coronary artery cannula — LivaNova USA, Inc. · Class II
- PEAK MEDICAL — PEAK MEDICAL Distribution Inc · Class I
- PEAK MEDICAL — PEAK MEDICAL Distribution Inc · Class I
- Coronary artery cannula — LivaNova USA, Inc. · Class II
- Edwards Lifesciences Retrograde Cardioplegia Catheter — Edwards Lifesciences LLC · Class II
- Coronary sinus cannula — LivaNova USA, Inc. · Class II
- PEAK MEDICAL — PEAK MEDICAL Distribution Inc · Class I
- Coronary artery cannula — LivaNova USA, Inc. · Class II
Cleared under the same submission
K123762 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medtronic, Inc.
Sources (1)
- FDA UDI 2e768f29-73dd-4df8-b20f-aa6a89799080 36 fields · synced May 30, 2026