← Back to catalogue

Weck

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
WECK FDA UDI
Generic Name
Surgical clip remover, reusable FDA UDI
Device Name
HEM-O-LOK 5MM ENDOSCOPIC CLIP REMOVER FDA UDI
Model / Reference
IPN915150 FDA UDI
Description
HEM-O-LOK 5MM ENDOSCOPIC CLIP REMOVER FDA UDI

Identifiers

Catalog Number
544121 FDA UDI
Primary DI / UDI-DI
24026704696677 FDA UDI
FDA Product Code
GDO FDA UDI
GMDN Term
Surgical clip remover, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Width — 5.09 Inch FDA UDI
Length — 17.21 Inch FDA UDI

Category: Surgical clip remover, reusable

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

Similar devices

Also classified as Surgical clip remover, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI d5834f7d-df18-47b6-bc82-a8ceac5a50d0 36 fields · synced Jun 1, 2026