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DYNATAPE Suture

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 280825Model DYNATAPE Suture

by Medos International SARL

Identity

Trade Name
DYNATAPE Suture EUDAMED
DYNATAPE FDA UDI
Generic Name
Polyolefin/fluoropolymer suture, multifilament FDA UDI
Device Name
DYNATAPE Suture, White, Black, Blue EUDAMED
DYNATAPE Suture White/Black Braided Flat Suture 2.5mm 36 inch (91cm) FDA UDI
Model / Reference
DYNATAPE Suture EUDAMED
280825 EUDAMEDFDA UDI
Description
DYNATAPE Suture White/Black Braided Flat Suture 2.5mm 36 inch (91cm) FDA UDI

Identifiers

Catalog Number
280825 FDA UDI
Primary DI / UDI-DI
20886705031198 EUDAMEDFDA UDI
Basic UDI-DI
0886705a00083KM EUDAMED
Unit of Use DI
10886705031191 EUDAMED
510(k) Number
K203186 FDA UDI
FDA Product Code
GAT FDA UDI
EMDN Code
H0102010299 SYNTHETIC NONABSORBABLE MULTIFILAMENT SUTURES - OTHER EUDAMED
GMDN Term
Polyolefin/fluoropolymer suture, multifilament FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.5000 FDA UDI
Market of Registration
Belgium 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

Sutures

Yes

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

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
MRI Safety
MR Safe FDA UDI

Category: Polyester suture, non-bioabsorbable, multifilament

DYNATAPE Suture by Medos International Sarl — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyester suture, non-bioabsorbable, multifilament.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
CH-MF-000014268
Authorised Representative
DePuy Ireland UC IE-AR-000009328

Sources (2)

  • EUDAMED 4edc4597-f0f0-4f4c-bc96-a7e645650258 61 fields · synced May 29, 2026
  • FDA UDI 6abce9e6-1abb-4719-8f18-e8bc997ec736 36 fields · synced May 29, 2026