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DYNACORD Suture, Braided Composite

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 222069Model DYNACORD Suture

by Medos International SARL

Identity

Trade Name
DYNACORD FDA UDI
Generic Name
Polyolefin/fluoropolymer suture, multifilament FDA UDI
Device Name
DYNACORD Suture, Braided Composite EUDAMED
DYNACORD Suture 1 Blue and 1 White/Blue/Green Striped Braided Composite Suture Number 2 (5 metric), 36 inches (91 cm) FDA UDI
Model / Reference
DYNACORD Suture EUDAMED
222069 EUDAMEDFDA UDI
Description
DYNACORD Suture 1 Blue and 1 White/Blue/Green Striped Braided Composite Suture Number 2 (5 metric), 36 inches (91 cm) FDA UDI

Identifiers

Catalog Number
222069 FDA UDI
Primary DI / UDI-DI
20886705030030 EUDAMEDFDA UDI
Basic UDI-DI
0886705a00053KC EUDAMED
Unit of Use DI
10886705030033 EUDAMED
510(k) Number
K181182 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

DYNACORD Suture, Braided Composite 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

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Manufacturer

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

Sources (2)

  • EUDAMED 832984e8-c385-401f-a688-e5e62084c536 61 fields · synced Jul 17, 2026
  • FDA UDI a0e98b2d-43f3-4833-bb5d-8423c0962d3e 36 fields · synced May 30, 2026