Philips Global Business Services LLP
Pune, IN
Philips Global Business Services LLP appears in FDA device records in Pune, IN. FDA records list no 510(k) clearances, no PMA records and 2 registered establishments. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
- 510(k) clearances
- 0
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 2
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3016851825 | 3016851825 | Philips Global Business Services LLP | B-78/B-79, MIDC, Pune Maharashtra 410501 IN | 2026 | |
| 3029227324 | 3029227324 | Philips Global Business Services LLP | 5th Floor, Amar Madhuban Tech Park, Baner Pune Maharashtra 411045 IN | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- PXPBreast Biopsy / Localization Tray
- MOSCoil, Magnetic Resonance, Specialty
- MNTContinuous, Minimal Ventilatory Support, Facility Use Ventilator
- NOUContinuous, Ventilator, Home Use
- NHJDevice, Positive Pressure Breathing, Intermittent
- CAWGenerator, Oxygen, Portable
- GDFGuide, Needle, Surgical
- BZEHeater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer
- NVPHolding Chambers, Direct Patient Interface
- CAFNebulizer (Direct Patient Interface)
- LNHSystem, Nuclear Magnetic Resonance Imaging
- LNISystem, Nuclear Magnetic Resonance Spectroscopic
- CBKVentilator, Continuous, Facility Use
- MNSVentilator, Continuous, Non-Life-Supporting
- BZDVentilator, Non-Continuous (Respirator)
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
