FDA Registration
Active
🇺🇸 United States
Biomedical Polymers, Inc.
Reg #: 1220502
·
FEI: 1220502
·
Expires 2026
Products
10
Proprietary Names
10
Establishment Types
5
Classifications
10
Registration Details
- Registration Name
- Biomedical Polymers, Inc.
- Registration Number
- 1220502
- FEI Number
- 1220502
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- 16 Chocksett Road
- City
- Sterling
- State
- MA
- ZIP
- 01564
- Country
- US
Owner / Operator
- Firm Name
- BIOMEDICAL POLYMERS, INC. dba BMP Medical
- Operator Number
- 9012278
- Address
- 16 Chocksett Rd., --
- City
- Sterling
- State
- MA
- Postal Code
- 01564
- Country
- US
- Correspondent
- MICHAEL T FAULKNER
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Kit, Screening, Urine | JXA | Class 1 | Microbiology | No | 2016-03-28 |
| Device, Transfer, Patient, Manual | FMR | Class 1 | General Hospital | No | 2019-04-11 |
| Container, Specimen, Urine, Drugs Of Abuse, Over The Counter | MPQ | Class 1 | Pathology | No | 2014-05-01 |
| Container, Specimen Mailer And Storage, Sterile | KDT | Class 1 | Pathology | No | 1997-07-03 |
| Grinder, Tissue | LEC | Class 1 | Pathology | No | 1997-07-03 |
| Container, Specimen, Non-Sterile | NNI | Class 1 | Pathology | No | 2025-02-24 |
| At Home Intravaginal Insemination System | QYZ | Class 2 | Obstetrics/Gynecology | No | 2024-07-30 |
| Slides, Microscope | KEW | Class 1 | Pathology | No | 2019-04-11 |
| Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use | LXG | Class 1 | Clinical Chemistry | No | 1995-01-23 |
| Filters, Cell Collection, Tissue Processing | KET | Class 1 | Pathology | No | 2011-09-26 |
Proprietary Names
urine test kit
Pipette
Urinalysis Examination Kit
Specimen, Container
TISSUE GRINDING SY
SPECIMEN COLLECTION COMMODE 32 OZ GRADUATED
Mosie Baby Kit
Decislide
Hemodrop
Cytology Funnel
Establishment Types
Manufacture Medical Device
Develop Specifications But Do Not Manufacture At This Facility
Complaint File Establishment per 21 CFR 820.198
Repack or Relabel Medical Device
Manufacture Medical Device for Another Party (Contract Manufacturer)