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Tevdek

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
TEVDEK FDA UDI
Generic Name
Polyester suture, non-bioabsorbable, multifilament FDA UDI
Device Name
Tevdek White Braided PTFE Impregnated Polyester Fiber Size 2-0 30" Two KT-3 Needles LSI FDA UDI
Model / Reference
IPN000925 FDA UDI
Description
Tevdek White Braided PTFE Impregnated Polyester Fiber Size 2-0 30" Two KT-3 Needles LSI FDA UDI

Identifiers

Catalog Number
LSI-100001 FDA UDI
Primary DI / UDI-DI
04026704605934 FDA UDI
FDA Product Code
GAT FDA UDI
GMDN Term
Polyester suture, non-bioabsorbable, multifilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5000 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Polyester suture, non-bioabsorbable, multifilament

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

Similar devices

Also classified as Polyester suture, non-bioabsorbable, multifilament.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI ed665f9d-032f-4d66-aa57-77bbdf926c4b 36 fields · synced Jun 6, 2026