← Back to catalogue

DemeLENE

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref PM290136F4P

by DemeTECH Corp

Identity

Trade Name
DemeLENE EUDAMEDFDA UDI
Generic Name
Polyolefin/fluoropolymer suture, monofilament FDA UDI
Device Name
DemeLENE EUDAMED
Synthetic (polypropylene), Non Absorbable Suture FDA UDI
Model / Reference
PM290136F4P EUDAMEDFDA UDI
Description
Synthetic (polypropylene), Non Absorbable Suture FDA UDI

Identifiers

Primary DI / UDI-DI
10652927291008 EUDAMEDFDA UDI
Basic UDI-DI
B-10652927291008 EUDAMED
510(k) Number
K043330 FDA UDI
FDA Product Code
GAW FDA UDI
EMDN Code
H010201010401 POLYPROPYLENE MONOFILAMENT WITH NEEDLE FOR OPEN SURGERY EUDAMED
GMDN Term
Polyolefin/fluoropolymer suture, monofilament FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.5010 FDA UDI
Market of Registration
Portugal EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Category: Polyolefin/fluoropolymer suture, monofilament

DemeLENE by DemeTECH Corp — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Polyolefin/fluoropolymer suture, monofilament.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
DemeTECH Corp

Sources (2)

  • FDA UDI 6ca0a397-7500-432c-8ca0-010e757c5dcb 36 fields · synced Oct 7, 2026
  • EUDAMED c054b0f1-5e57-4565-9ed3-e758de3fc523 61 fields · synced Oct 7, 2026