Identity
- Trade Name
- BD Alaris™ PCU Module, Model 8015 FDA UDI
- Generic Name
- Bedside infusion pump, single-channel FDA UDI
- Device Name
- BD Alaris™ PCU Module, Model 8015 v12.3.1 FDA UDI
- Model / Reference
- 8015 FDA UDI
- Description
- BD Alaris™ PCU Module, Model 8015 v12.3.1 FDA UDI
Identifiers
- Catalog Number
- 8015BDCDXEN1231 FDA UDI
- Primary DI / UDI-DI
- 10885403516023 FDA UDI
- FDA Product Code
- FRN FDA UDI
- GMDN Term
- Bedside infusion pump, single-channel FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5725 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Bedside infusion pump, single-channel
BD Alaris™ PCU Module, Model 8015 by CareFusion 303, INC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bedside infusion pump, single-channel.
- Klein Tumescent Infiltration Pump — HK SURGICAL INC. · Class II
- CADD — ICU MEDICAL, INC. · Class II
- Sapphire Epidural Infusion Kit - US — EITAN MEDICAL LTD · Class II
- Plum — Hospira, Inc. · Class II
- Plum — Hospira, Inc. · Class II
- ICU Medical, INC. — ICU MEDICAL, INC. · Class II
- CADD — ICU MEDICAL, INC. · Class II
- Dispenser DP 30 — Nouvag AG · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- CareFusion 303, INC
Sources (1)
- FDA UDI a33cde58-c557-4dec-a1b7-265cec3241e1 36 fields · synced Jun 1, 2026