Identity
- Trade Name
- SILHOUETTE CIRCUIT,PEDIATRIC,1 FDA UDI
- Generic Name
- Anaesthesia face mask, reusable FDA UDI
- Device Name
- SILHOUETTE CIRCUIT,PEDIATRIC,1 FDA UDI
- Model / Reference
- SIL-PEDO-12 FDA UDI
- Description
- SILHOUETTE CIRCUIT,PEDIATRIC,1 FDA UDI
Identifiers
- Catalog Number
- SIL-PEDO-12 FDA UDI
- Primary DI / UDI-DI
- 00816711021865 FDA UDI
- FDA Product Code
- CAI FDA UDI
- GMDN Term
- Anaesthesia face mask, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5240 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Anaesthesia face mask, reusable
Silhouette Circuit, Pediatric, 1 by Parker Hannifin Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Anaesthesia face mask, reusable.
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- AincA® — Anesthesia Associates, Inc. · Class I
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
- Parker Hannifin Corp.
Sources (1)
- FDA UDI b3f0d3c8-9bb8-4cef-bf2a-03f405380d2d 34 fields · synced Jun 8, 2026