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T-DOC 5Fr Air-Charged Single Sensor Catheter

FDA UDI

Class II (US FDA UDI)

by Laborie Medical Technologies Corp.

Identity

Trade Name
T-DOC 5Fr Air-Charged Single Sensor Catheter FDA UDI
Generic Name
Urodynamic manometric catheter, electronic, single-use FDA UDI
Device Name
T-DOC 5Fr Air-Charged Single Sensor Catheter FDA UDI
Model / Reference
CAT595P FDA UDI
Description
T-DOC 5Fr Air-Charged Single Sensor Catheter FDA UDI

Identifiers

Primary DI / UDI-DI
10627825014851 FDA UDI
FDA Product Code
FEN FDA UDI
GMDN Term
Urodynamic manometric catheter, electronic, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1620 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Urodynamic manometric catheter, electronic, single-use

T-DOC 5Fr Air-Charged Single Sensor Catheter by Laborie Medical Technologies Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urodynamic manometric catheter, electronic, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e211e266-77ac-426c-b9b7-e079fdfd6594 33 fields · synced Jun 9, 2026