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Taut

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
TAUT FDA UDI
Generic Name
Surgical capillary wound drain, luminal, synthetic polymer FDA UDI
Device Name
TAUT CAPILLARY DRAINS 20/BX LATEX FREE 12X3/8 FDA UDI
Model / Reference
IPN004356 FDA UDI
Description
TAUT CAPILLARY DRAINS 20/BX LATEX FREE 12X3/8 FDA UDI

Identifiers

Catalog Number
20426-537C FDA UDI
Primary DI / UDI-DI
04026704419005 FDA UDI
FDA Product Code
FFA FDA UDI
GMDN Term
Surgical capillary wound drain, luminal, synthetic polymer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5090 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 12 Inch FDA UDI
Width — 0.375 Inch FDA UDI

Category: Surgical capillary wound drain, luminal, synthetic polymer

Taut by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical capillary wound drain, luminal, synthetic polymer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 89796afe-00a1-459a-9a57-c2fbbab0bae1 36 fields · synced Jun 8, 2026