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Deknatel

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
DEKNATEL FDA UDI
Generic Name
Polyglycolic acid suture FDA UDI
Device Name
DK LK BON+1 C-7 7-4" 2L FDA UDI
Model / Reference
IPN009329 FDA UDI
Description
DK LK BON+1 C-7 7-4" 2L FDA UDI

Identifiers

Catalog Number
6-6038 FDA UDI
Primary DI / UDI-DI
04026704419265 FDA UDI
FDA Product Code
GAM FDA UDI
GMDN Term
Polyglycolic acid suture FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4493 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Length — 90 Centimeter FDA UDI

Category: Polyglycolic acid suture

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

Similar devices

Also classified as Polyglycolic acid suture.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 4f826d58-94f7-4d79-932c-056a2dc4331b 36 fields · synced May 30, 2026