Identity
- Trade Name
- INTERLINK/DUO-VENT FDA UDI
- Generic Name
- Basic intravenous administration set, noninvasive FDA UDI
- Device Name
- Non-DEHP Secondary Medication Set with DUO-VENT Spike, Hanger, Lever Lock Cannula, Male Luer Lock Adapter FDA UDI
- Model / Reference
- 2H7452 FDA UDI
- Description
- Non-DEHP Secondary Medication Set with DUO-VENT Spike, Hanger, Lever Lock Cannula, Male Luer Lock Adapter FDA UDI
Identifiers
- Catalog Number
- 2H7452 FDA UDI
- Primary DI / UDI-DI
- 00085412068664 FDA UDI
- 510(k) Number
- K123868 FDA UDI
- FDA Product Code
- FPA FDA UDI
- GMDN Term
- Basic intravenous administration set, noninvasive FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5440 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Basic intravenous administration set, noninvasive
Interlink/Duo-Vent by Baxter International Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Basic intravenous administration set, noninvasive.
- Merit Medical® — Merit Medical Systems, Inc. · Class II
- ICU Medical — ICU MEDICAL, INC. · Class II
- ICU Medical — ICU MEDICAL, INC. · Class II
- IMED — BQ PLUS MEDICAL CO., LTD. · Class II
- ICU Medical — ICU MEDICAL, INC. · Class II
- ICU Medical — ICU MEDICAL, INC. · Class II
- Kew Medical — DOUGLAS MEDICAL PRODUCTS, INC · Class II
- ICU Medical — ICU MEDICAL, INC. · Class II
Cleared under the same submission
K123868 also covers:
- INTERLINK — BAXTER INTERNATIONAL INC.
- INTERLINK — BAXTER INTERNATIONAL INC.
- INTERLINK — BAXTER INTERNATIONAL INC.
- INTERLINK — BAXTER INTERNATIONAL INC.
- INTERLINK — BAXTER INTERNATIONAL INC.
- INTERLINK/CONTINU-FLO — BAXTER INTERNATIONAL INC.
- INTERLINK/CONTINU-FLO — BAXTER INTERNATIONAL INC.
- INTERLINK/CONTINU-FLO — BAXTER INTERNATIONAL INC.
- INTERLINK/CONTINU-FLO — BAXTER INTERNATIONAL INC.
- INTERLINK/CONTINU-FLO/DUO-VENT — BAXTER INTERNATIONAL INC.
- INTERLINK/DUO-VENT — BAXTER INTERNATIONAL INC.
- INTERLINK — Baxter Healthcare Corp
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
- Baxter International Inc.
Sources (1)
- FDA UDI 08e527b3-95d4-49ea-9a2c-ce254c86949f 36 fields · synced May 30, 2026