Identity
- Trade Name
- 1A CHAMBER FDA UDI
- Generic Name
- Medicine chamber spacer, reusable FDA UDI
- Device Name
- PREMIUM VALVE HOLDING CHAMBER WITH MOUTHPIECE FDA UDI
- Model / Reference
- MOUTHPIECE FDA UDI
- Description
- PREMIUM VALVE HOLDING CHAMBER WITH MOUTHPIECE FDA UDI
Identifiers
- Catalog Number
- 10404 FDA UDI
- Primary DI / UDI-DI
- B91710404 FDA UDI
- FDA Product Code
- CCQ FDA UDI
- GMDN Term
- Medicine chamber spacer, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5640 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Medicine chamber spacer, reusable
1a Chamber by Patejim S.r.l. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Patejim S.r.l.
Sources (1)
- FDA UDI 64d203f6-a7d2-4b1a-a4ce-da6f202f959d 34 fields · synced Jun 6, 2026