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Grid Plate- Enhanced Access- Med. For Invivo Breast Biopsy System
EUDAMEDFDA UDIClass I (EU MDR)
Ref 989603209123
Identity
- Trade Name
- Grid Plate- Enhanced Access- Med. For Invivo Breast Biopsy System EUDAMEDInvivo FDA UDI
- Generic Name
- Needle guide, single-use FDA UDI
- Device Name
- Breast Biopsy Guidance Devices EUDAMEDGrid Plate, Enhanced Access, med. FDA UDI
- Model / Reference
- 989603209123 EUDAMEDGrid Plate, Enhanced Access, Med FDA UDI
- Description
- Grid Plate, Enhanced Access, med. FDA UDI
Identifiers
- Catalog Number
- 989603209123 FDA UDI
- Primary DI / UDI-DI
- 00884838073142 EUDAMEDFDA UDI
- Basic UDI-DI
- 0884838BM421SN EUDAMED
- FDA Product Code
- GDF FDA UDI
- EMDN Code
- A018002 NEEDLE GUIDES EUDAMED
- GMDN Term
- Needle guide, single-use FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
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
No
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
MR Conditional FDA UDI
Grid Plate- Enhanced Access- Med. For Invivo Breast Biopsy System by Invivo Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union No Longer Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0884838BM421SN | Class I | No Longer Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Invivo Corporation
- EUDAMED SRN
- US-MF-000002284
- Authorised Representative
- Philips Medical Systems Nederland B.V. NL-AR-000001422
Sources (2)
- EUDAMED ad5851dd-e888-4b7c-8026-f0dc87857d6d 61 fields · synced Jul 8, 2026
- FDA UDI 0bea9bb8-3b83-417d-bf81-42dba1f7c8eb 36 fields · synced May 30, 2026