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Deknatel

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
DEKNATEL FDA UDI
Generic Name
Polyester suture, non-bioabsorbable, multifilament FDA UDI
Device Name
READI-CUT TEVDEK GREEN BRAIDED SIZE 2 24 INCHES FDA UDI
Model / Reference
IPN914877 FDA UDI
Description
READI-CUT TEVDEK GREEN BRAIDED SIZE 2 24 INCHES FDA UDI

Identifiers

Catalog Number
122-TR FDA UDI
Primary DI / UDI-DI
14026704673183 FDA UDI
510(k) Number
K153089 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

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

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

Deknatel 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.

Cleared under the same submission

K153089 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 545c8974-d751-480e-bed4-bfc67a5faf76 36 fields · synced Jun 1, 2026