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Deknatel

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
DEKNATEL FDA UDI
Generic Name
Metallic suture, monofilament FDA UDI
Device Name
STL MF 5 K-60 1N 30 FDA UDI
Model / Reference
IPN004791 FDA UDI
Description
STL MF 5 K-60 1N 30 FDA UDI

Identifiers

Catalog Number
29-727 FDA UDI
Primary DI / UDI-DI
14026704419545 FDA UDI
FDA Product Code
GAQ FDA UDI
GMDN Term
Metallic suture, monofilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4495 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 75 Centimeter FDA UDI

Category: Metallic suture, monofilament

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

Similar devices

Also classified as Metallic suture, monofilament.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI a44d64e9-4c1d-4c91-9454-63cf8e0ac656 36 fields · synced May 30, 2026