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Symphony™ Clot Container

FDA UDI

Class II (US FDA UDI)

by Imperative Care Inc.

Identity

Trade Name
Symphony™ Clot Container FDA UDI
Generic Name
Thrombectomy suction catheter FDA UDI
Device Name
Symphony Clot Container FDA UDI
Model / Reference
SYMPHONYCC FDA UDI
Description
Symphony Clot Container FDA UDI

Identifiers

Catalog Number
SYMPHONYCC FDA UDI
Primary DI / UDI-DI
00850032079167 FDA UDI
510(k) Number
K223216 FDA UDI
K250775 FDA UDI
K252057 FDA UDI
FDA Product Code
QEW FDA UDI
KRA FDA UDI
GMDN Term
Thrombectomy suction catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5150 FDA UDI
870.1210 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Thrombectomy suction catheter

Symphony™ Clot Container by Imperative Care Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thrombectomy suction catheter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b5b175ea-0762-48d6-8775-3fb048335e02 37 fields · synced May 30, 2026