Identity
- Trade Name
- RPC FDA UDI
- Generic Name
- Haemodialysis blood tubing set, single-use FDA UDI
- Device Name
- Recirculation Connector FDA UDI
- Model / Reference
- 7001-3902W FDA UDI
- Description
- Recirculation Connector FDA UDI
Identifiers
- Catalog Number
- 7001-3902W FDA UDI
- Primary DI / UDI-DI
- 00858293006007 FDA UDI
- 510(k) Number
- K852605 FDA UDI
- FDA Product Code
- FJK FDA UDI
- GMDN Term
- Haemodialysis blood tubing set, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5820 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
Category: Haemodialysis blood tubing set, single-use
Rpc by Reprocessing Products Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Haemodialysis blood tubing set, single-use.
- 10" Dialysis Tubing Extensions (Pair) — Cardio Med Supplies, Inc. · Class II
- CombiSet — Fresenius Medical Care Holdings, Inc. · Class II
- Hemodialysis Bloodlines — B. BRAUN MEDICAL INC. · Class II
- SAMI Hemofiltration Cassette — Dialco Medical Inc · Class II
- 5008X — Fresenius Medical Care Renal Therapies Group, LLC · Class II
- NIPRO SET BLOOD TUBING SET WITH TRANSDUCER PROTECTORS AND PRIMING SET — NIPRO MEDICAL CORPORATION · Class II
- Nipro Set Blood Tubing Set — NIPRO MEDICAL CORPORATION · Class II
- Molded Products, Inc. — MOLDED PRODUCTS INC. · Class II
Cleared under the same submission
K852605 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
- Reprocessing Products Corp
Sources (1)
- FDA UDI 0cb998bb-a40e-4437-9a0d-1403473e7126 35 fields · synced Jun 8, 2026