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Argus Pb-3000
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref 3.921000Model ARGUS PB-3000
by Schiller Ag
Identity
- Trade Name
- ARGUS PB-3000 EUDAMEDFDA UDI
- Generic Name
- Patient monitoring system module, multifunction FDA UDI
- Device Name
- The ARGUS PB-3000 is a vital data acquisition unit intended to be used within or connected to a medical device or a medical System (Host System) for acquiring, analysing, and transmission of patient vitals and other pertinent clinical data. FDA UDI
- Model / Reference
- ARGUS PB-3000 EUDAMED3.921000 EUDAMEDPB-3000 Var.2, sub-variant: S FDA UDI
- Description
- The ARGUS PB-3000 is a vital data acquisition unit intended to be used within or connected to a medical device or a medical System (Host System) for acquiring, analysing, and transmission of patient vitals and other pertinent clinical data. FDA UDI
Identifiers
- Catalog Number
- 3.921000 FDA UDI
- Primary DI / UDI-DI
- 07613365001846 EUDAMEDFDA UDI
- Basic UDI-DI
- 76133650000000014U EUDAMED
- 510(k) Number
- K221056 FDA UDI
- FDA Product Code
- MHX FDA UDI
- EMDN Code
- Z1203020299 MULTI–PARAMETER MONITORS - OTHER EUDAMED
- GMDN Term
- Patient monitoring system module, multifunction FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 870.1025 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
MR Unsafe FDA UDI
Argus Pb-3000 by Schiller AG — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 76133650000000014U | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Schiller Ag
- EUDAMED SRN
- CH-MF-000012722
- Authorised Representative
- SCHILLER Medizintechnik GmbH DE-AR-000006934
Sources (2)
- EUDAMED cb9a111c-0529-40b7-983e-5dbce1da6738 61 fields · synced Jul 10, 2026
- FDA UDI 76f6546d-2e31-432f-83d8-6e60fefab1b5 37 fields · synced May 30, 2026