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Weck

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
WECK FDA UDI
Generic Name
Ligation clip, synthetic polymer, non-bioabsorbable FDA UDI
Device Name
HOL PURPLEPLUS L CLIPS 6/CART 84/BOX FDA UDI
Model / Reference
IPN928663 FDA UDI
Description
HOL PURPLEPLUS L CLIPS 6/CART 84/BOX FDA UDI

Identifiers

Catalog Number
HOL2LG FDA UDI
Primary DI / UDI-DI
14026704921321 FDA UDI
510(k) Number
K251054 FDA UDI
FDA Product Code
FZP FDA UDI
GMDN Term
Ligation clip, synthetic polymer, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Ligation clip, synthetic polymer, non-bioabsorbable

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

Similar devices

Also classified as Ligation clip, synthetic polymer, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 8127f2b4-6727-4a97-8567-46347f25426e 36 fields · synced May 30, 2026