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Whipknot

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
WHIPKNOT FDA UDI
Generic Name
Ligation clip, synthetic polymer, non-bioabsorbable FDA UDI
Device Name
WHIPKNOT, No.5 SOFT TISSUE CINCH, STERILE 1 PER BOX FDA UDI
Model / Reference
7211015 FDA UDI
Description
WHIPKNOT, No.5 SOFT TISSUE CINCH, STERILE 1 PER BOX FDA UDI

Identifiers

Catalog Number
7211015 FDA UDI
Primary DI / UDI-DI
03596010514943 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Ligation clip, synthetic polymer, non-bioabsorbable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

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

No

FDA UDI

Category: Ligation clip, synthetic polymer, non-bioabsorbable

Whipknot by Smith & Nephew, Inc. — Class I — 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
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI 8765644d-7d57-42ce-a62e-f12975e9c783 35 fields · synced Jun 8, 2026