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InHealth Technologies

FDA UDI

Class II (US FDA UDI)

by Freudenberg Medical, Llc

Identity

Trade Name
InHealth Technologies FDA UDI
Generic Name
Tracheoesophageal speech valve, indwelling FDA UDI
Model / Reference
VP 2208-LEF FDA UDI

Identifiers

Primary DI / UDI-DI
00848253003672 FDA UDI
FDA Product Code
EWL FDA UDI
GMDN Term
Tracheoesophageal speech valve, indwelling FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Category: Tracheoesophageal device insertion capsuleTracheoesophageal device introducerTracheoesophageal speech valve, indwelling

InHealth Technologies by Freudenberg Medical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tracheoesophageal speech valve, indwelling.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3ae738c1-8d79-479f-a919-0347fd30031a 34 fields · synced Sep 18, 2026