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TRUCLEARTM Control Unit

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
TRUCLEARTM Control Unit FDA UDI
Generic Name
Tissue morcellation system control unit FDA UDI
Device Name
SVCE REPL CU HYSTER MORCELLATION FDA UDI
Model / Reference
7209808S FDA UDI
Description
SVCE REPL CU HYSTER MORCELLATION FDA UDI

Identifiers

Catalog Number
7209808S FDA UDI
Primary DI / UDI-DI
00885556570340 FDA UDI
FDA Product Code
HIH FDA UDI
GMDN Term
Tissue morcellation system control unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1690 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tissue morcellation system control unit

TRUCLEARTM Control Unit by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue morcellation system control unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 58daad3a-7ffc-4c19-bacf-17b59f96f965 35 fields · synced Jun 8, 2026