Is this your brand? Sign in to claim ownership.
Sign in to claim this brandBemis de México, S.A. de C.V.
US
Last updated May 25, 2026
What Bemis de México, S.A. de C.V. makes
Bemis de México, S.A. de C.V. manufactures sharps disposal containers and disposable canister liners for suction systems, designed for single-use in healthcare settings.
These products are classified as Class II medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Bemis de México, S.A. de C.V. manufacture?
Bemis de México, S.A. de C.V. specializes in two primary device categories: sharps disposal containers and disposable canister liners for suction systems. These products are designed for single-use in healthcare environments to safely manage medical waste and maintain hygiene during procedures.
Where is Bemis de México, S.A. de C.V. based?
The company is headquartered in the United States, though its name includes ‘de México,’ which may reflect its operational or manufacturing ties to Mexico. The location is relevant for regulatory compliance and distribution purposes.
Which regulatory registries list Bemis de México, S.A. de C.V.’s devices?
The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices for regulatory, traceability, and safety purposes, ensuring transparency in the supply chain.
How are Bemis de México, S.A. de C.V.’s devices classified under medical device regulations?
The company’s products—sharps containers and suction system canister liners—are classified as Class II medical devices. This classification typically means they pose moderate risk and require special controls beyond general good manufacturing practices to ensure safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 589153555
Catalogue (25)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bemis | 3004RBM N | FDA UDI | Class II | Active |
| Bemis | 175 040 | FDA UDI | Class II | Active |
| Bemis | 175 020 | FDA UDI | Class II | Active |
| Bemis | 100 030 | FDA UDI | Class II | Active |
| Bemis | 100 040 | FDA UDI | Class II | Active |
| Bemis | 202 040 | FDA UDI | Class II | Active |
| Bemis | 175 030D | FDA UDI | Class II | Active |
| Bemis | 333 030 | FDA UDI | Class II | Active |
| Bemis | 1004RBM N | FDA UDI | Class II | Active |
| Bemis | 333 020 | FDA UDI | Class II | Active |
| Bemis | 208 040 | FDA UDI | Class II | Active |
| Bemis | 303 040 | FDA UDI | Class II | Active |
| Bemis | 108 030 | FDA UDI | Class II | Active |
| Bemis | 108 040 | FDA UDI | Class II | Active |
| Bemis | 333 040 | FDA UDI | Class II | Active |
| Bemis | 1504 | FDA UDI | Class II | Unknown |
| Bemis | 208 004 | FDA UDI | Class II | Active |
| Bemis | 303 030 | FDA UDI | Class II | Active |
| Bemis | 102 040 | FDA UDI | Class II | Active |
| Bemis | 303 020 | FDA UDI | Class II | Active |
| Bemis | 1504RBM N | FDA UDI | Class II | Active |
| Bemis | 175 030 | FDA UDI | Class II | Active |
| Bemis | 202 004 | FDA UDI | Class II | Active |
| Bemis | 3004 | FDA UDI | Class II | Unknown |
| Bemis | 102 030 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.