Silhouette 2 Circuit, Pedo, 24 Pk

FDA UDI

Class I (US FDA UDI)

by Parker Hannifin Corp.

Identity

Trade Name: SILHOUETTE 2 CIRCUIT,PEDO,24 PK FDA UDI
Generic Name: Anaesthesia breathing circuit, single-use FDA UDI
Device Name: SILHOUETTE 2 CIRCUIT,PEDO,24 PK FDA UDI
Model / Reference: SIL2-PEDO-24 FDA UDI
Description: SILHOUETTE 2 CIRCUIT,PEDO,24 PK FDA UDI

Identifiers

Catalog Number: SIL2-PEDO-24 FDA UDI
Primary DI / UDI-DI: 00816711024088 FDA UDI
FDA Product Code: CAI FDA UDI
GMDN Term: Anaesthesia breathing circuit, single-use 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Anaesthesia breathing circuit, single-use

Silhouette 2 Circuit, Pedo, 24 Pk by Parker Hannifin Corp. — 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: Parker Hannifin Corp.

Sources (1)

FDA UDI 6192ee1e-6072-459f-a6e0-1a256392640b 34 fields · synced May 30, 2026