Identity
- Trade Name
- Mariner FDA UDI
- Generic Name
- Angiographic catheter, single-use FDA UDI
- Device Name
- Mariner Hydrophilic Coated Angiographic Catheter, Berenstein, Non-Braided FDA UDI
- Model / Reference
- 11722109 FDA UDI
- Description
- Mariner Hydrophilic Coated Angiographic Catheter, Berenstein, Non-Braided FDA UDI
Identifiers
- Primary DI / UDI-DI
- H787117221090 FDA UDI
- FDA Product Code
- DQO FDA UDI
- GMDN Term
- Angiographic catheter, single-use 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
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
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 130 Centimeter FDA UDICatheter Gauge — 5 French FDA UDI
Category: Angiographic catheter, single-use
Mariner by Angiodynamics, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K112452 also covers:
- AccuVu — ANGIODYNAMICS, INC
- AccuVu — ANGIODYNAMICS, INC
- AccuVu — ANGIODYNAMICS, INC
- AngiOptic — ANGIODYNAMICS, INC
- AngiOptic — ANGIODYNAMICS, INC
- AngiOptic — ANGIODYNAMICS, INC
- AngiOptic — ANGIODYNAMICS, INC
- AngiOptic — ANGIODYNAMICS, INC
- AngiOptic — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
K161596 also covers:
- AccuVu — ANGIODYNAMICS, INC
- AccuVu — ANGIODYNAMICS, INC
- AngiOptic — ANGIODYNAMICS, INC
- AngiOptic — ANGIODYNAMICS, INC
- AngiOptic — ANGIODYNAMICS, INC
- AngiOptic — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
K173762 also covers:
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
- Mariner — ANGIODYNAMICS, INC
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
- Angiodynamics, Inc
Sources (1)
- FDA UDI 1c1fe2bc-e2cc-45be-a1d8-ab4a445040e9 37 fields · synced Jun 20, 2026