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Sign in to claim this brandPATEJIM S.R.L.
US
Last updated May 30, 2026
What PATEJIM S.R.L. makes
Patejim S.R.L. manufactures reusable medicine chamber spacers designed to assist in the administration of inhaled medications. These devices are intended to improve the delivery of aerosolized drugs by holding the medication between the inhaler and the user’s mouth.
The company’s products fall under Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 Patejim S.R.L. manufacture?
Patejim S.R.L. specializes in reusable medicine chamber spacers. These devices are designed to help improve the delivery of inhaled medications by acting as a spacer between the inhaler and the user’s mouth, ensuring the medication is properly dispersed before inhalation.
Where is Patejim S.R.L. based?
Patejim S.R.L. is based in the United States. The company’s location is relevant for regulatory compliance and customer inquiries, as it operates within the U.S. healthcare system.
How are Patejim S.R.L.’s devices classified under medical device regulations?
Patejim S.R.L.’s medicine chamber spacers fall under Class I medical devices. This classification is typically assigned to low-risk devices that pose minimal risk to patients, such as reusable spacers for inhaled medications, which do not require invasive procedures or significant regulatory oversight beyond basic manufacturing controls.
Are Patejim S.R.L.’s devices listed in any regulatory registries?
Yes, Patejim S.R.L.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. Listing in the UDI system ensures traceability and transparency in the supply chain, allowing healthcare providers and regulators to verify device details, such as manufacturer information and device identifiers, for compliance and safety tracking.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 975299082
Catalogue (5)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| 1a Chamber | YOUTH | FDA UDI | Class I | Active |
| 1a Chamber | MOUTHPIECE | FDA UDI | Class I | Active |
| 1a Chamber | BREASTFEEDING BABY | FDA UDI | Class I | Active |
| 1a Chamber | ADULT | FDA UDI | Class I | Active |
| 1a Chamber | INFANT | FDA UDI | Class I | Active |
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