Bausch+Lomb Netherlands B.V. Amsterdam Logistics Centre
SCHIPOL RIJK Noord-Holland, NL
Bausch+Lomb Netherlands B.V. Amsterdam Logistics Centre appears in FDA device records in SCHIPOL RIJK Noord-Holland, NL. FDA records list no 510(k) clearances, no PMA records and one registered establishment. 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
- 1
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 |
|---|---|---|---|---|---|
| 3003365815 | 3003365815 | Bausch+Lomb Netherlands B.V. Amsterdam Logistics Centre | KOOLHOVENLAAN 110, SCHIPOL RIJK Noord-Holland 1119 NH NL | 2026 | and 4 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- HMXCannula, Ophthalmic
- OJKEye Tray
- LWLFluid, Intraocular
- MSSFolders And Injectors, Intraocular Lens (Iol)
- HNRForceps, Ophthalmic
- HNQHook, Ophthalmic
- MVNLens, Contact, (Disposable)
- KYBLens, Guide, Intraocular
- LPLLenses, Soft Contact, Daily Wear
- LPMLenses, Soft Contact, Extended Wear
- GXIProbe, Radiofrequency Lesion
- HNDSpatula, Ophthalmic
- HNCSpecula, Ophthalmic
- HQCUnit, Phacofragmentation
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
