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Weck

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 544130

by Teleflex Incorporated

Identity

Trade Name
HEM-O-LOK REMOVER, EXTRA LARGE/LARGE ENDOSCOPIC EUDAMED
WECK FDA UDI
Generic Name
Surgical clip remover, reusable FDA UDI
Device Name
Weck® Hem-o-lok® Endoscopic Clip Removers, various sizes EUDAMED
HEM-O-LOK REMOVER, EXTRA LARGE/LARGE ENDOSCOPIC FDA UDI
Model / Reference
544130 EUDAMED
IPN921592 FDA UDI
Description
HEM-O-LOK REMOVER, EXTRA LARGE/LARGE ENDOSCOPIC FDA UDI

Identifiers

Catalog Number
544130 FDA UDI
Primary DI / UDI-DI
14026704727343 EUDAMEDFDA UDI
Basic UDI-DI
08019020000000000000007K6 EUDAMED
Direct Marketing DI
44026704727344 EUDAMED
FDA Product Code
GDO FDA UDI
EMDN Code
L21 CLIP REMOVAL SURGICAL FORCEPS, REUSABLE EUDAMED
GMDN Term
Surgical clip remover, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 32 Centimeter FDA UDI

Category: Surgical clip remover, reusable

Weck by Teleflex Incorporated — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical clip remover, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI e1499bfc-7490-4dc5-9505-0060771634f6 36 fields · synced Jul 18, 2026
  • EUDAMED b49d638c-af40-44f6-8b21-fb0e94aa3629 61 fields · synced Jul 18, 2026