Identity
- Trade Name
- Invivo FDA UDI
- Generic Name
- Needle guide, single-use FDA UDI
- Device Name
- Lateral Grid, Lower Breast dS 16ch I/T FDA UDI
- Model / Reference
- Lateral Grid, Lower dS Breast 16CH I/T FDA UDI
- Description
- Lateral Grid, Lower Breast dS 16ch I/T FDA UDI
Identifiers
- Catalog Number
- 989603210902 FDA UDI
- Primary DI / UDI-DI
- 00884838084407 FDA UDI
- FDA Product Code
- MOS FDA UDI
- GMDN Term
- Needle guide, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1000 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Category: Needle guide, single-use
Invivo by Philips DS North America LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Manufacturer
- Philips DS North America LLC
Sources (1)
- FDA UDI b1c1f858-8ce6-4637-847b-3e35a548f0f2 36 fields · synced Jun 8, 2026