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Deknatel

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
DEKNATEL FDA UDI
Generic Name
Polyolefin/fluoropolymer suture, monofilament FDA UDI
Device Name
DEK MX BL MF 3-0 C-2 2N 36"X4 PSL FDA UDI
Model / Reference
IPN011195 FDA UDI
Description
DEK MX BL MF 3-0 C-2 2N 36"X4 PSL FDA UDI

Identifiers

Catalog Number
CD-7042M4K FDA UDI
Primary DI / UDI-DI
04026704590544 FDA UDI
FDA Product Code
GAW FDA UDI
GMDN Term
Polyolefin/fluoropolymer suture, monofilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5010 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

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Length — 90 Centimeter FDA UDI

Category: Polyolefin/fluoropolymer suture, monofilament

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

Similar devices

Also classified as Polyolefin/fluoropolymer suture, monofilament.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dc148599-21c7-4943-b4d8-e98f53b9c502 36 fields · synced May 30, 2026