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Dormo-Strip

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref VE-022

by Telic, S.A.U.

Identity

Trade Name
Dormo-Strip EUDAMEDFDA UDI
Generic Name
Vein stripper, single-use FDA UDI
Device Name
Vein strippers EUDAMED
Vein strippers are single use medical devices, sterilized by Ethylene Oxide, intended to be used for surgical stripping of varicose veins. This product is not intended to be used in the central venous system. Model VE-022 model is intended for conventional stripping procedures. FDA UDI
Model / Reference
VE-022 EUDAMEDFDA UDI
Description
Vein strippers are single use medical devices, sterilized by Ethylene Oxide, intended to be used for surgical stripping of varicose veins. This product is not intended to be used in the central venous system. Model VE-022 model is intended for conventional stripping procedures. FDA UDI

Identifiers

Catalog Number
TCSS1 FDA UDI
Primary DI / UDI-DI
08427734036921 EUDAMEDFDA UDI
Basic UDI-DI
8427734VEINSTRIPPERSZP EUDAMED
FDA Product Code
GAJ FDA UDI
EMDN Code
C0699 CARDIOVASCULAR SURGERY INSTRUMENTS, SINGLE-USE - OTHER EUDAMED
GMDN Term
Vein stripper, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical bulldog clamp, single-use

Dormo-Strip by Telic, S.A.U. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical bulldog clamp, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Telic, S.A.U.
EUDAMED SRN
ES-MF-000001853

Sources (2)

  • EUDAMED 868f2e39-960f-4830-9c56-25f5b78c7d32 61 fields · synced Jun 20, 2026
  • FDA UDI ab722677-077b-496a-b338-9eb7b0ecc21d 35 fields · synced May 30, 2026