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Anivia SG1000 Pump Console
FDA UDIClass II (US FDA UDI)
by Asia Pacific Medical Technology Development Company Limited
Identity
- Trade Name
- Anivia SG1000 Pump Console FDA UDI
- Generic Name
- Cardiopulmonary bypass system centrifugal pump drive unit FDA UDI
- Device Name
- Backup Battery Module FDA UDI
- Model / Reference
- SG1000-BBM-001 FDA UDI
- Description
- Backup Battery Module FDA UDI
Identifiers
- Catalog Number
- SG1000-BBM-001 FDA UDI
- Primary DI / UDI-DI
- 04897102200065 FDA UDI
- FDA Product Code
- DWA FDA UDI
- GMDN Term
- Cardiopulmonary bypass system centrifugal pump drive unit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4380 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
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Cardiopulmonary bypass system centrifugal pump drive unit
Anivia SG1000 Pump Console by Asia Pacific Medical Technology Development Company Limited — Class II — FDA UDI — listed in FDA GUDID
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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 |
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Manufacturer
Sources (1)
- FDA UDI 0910c06a-df69-4a3e-95c4-73226e0f987e 36 fields · synced Jun 8, 2026