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Perchik Button™

FDA UDI

Class I (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
Perchik Button™ FDA UDI
Generic Name
Suture retention device FDA UDI
Model / Reference
A FDA UDI

Identifiers

Catalog Number
H787138002015 FDA UDI
Primary DI / UDI-DI
10884450786199 FDA UDI
FDA Product Code
KGS FDA UDI
GMDN Term
Suture retention device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4930 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Suture retention device

Perchik Button (Device ID: 33519) is a single-use, active suture retention device designed to aid wound healing by distributing suture tension over a larger area on the skin. This device is typically in the form of a retention bridge, surgical button, or suture bolster through which sutures are passed, helping prevent them from cutting the skin.

Similar devices

Also classified as Suture retention device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1b7e9b46-d0c6-46ef-a1eb-d6d4e726f1bc 33 fields · synced Jul 14, 2026