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CathGrip 51301

by Argentum Medical, LLC

CathGrip 51301 (BOM51301BX) is a wearable percutaneous catheter/tube holder (FDA Class I; FDA product code KMK, Device, Intravascular Catheter Securement) made by Argentum Medical, LLC, listed in FDA GUDID since 7 Jan 2020 (UDI-DI 00653599000410), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00653599000410 UDI-DI Date7 Jan 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
CathGrip
Generic name
Wearable percutaneous catheter/tube holder, single-use
Model / Ref / Catalog
51301, BOM51301BX
Primary DI / UDI-DI
00653599000410
FDA product code
KMK
GMDN term
Wearable percutaneous catheter/tube holder, single-use
Device class
Class I
Regulation number
880.5210
GUDID distribution status
In Commercial Distribution

Related devices

Category: Wearable percutaneous catheter/tube holder

Similar devices in this category

Other devices filed under Wearable percutaneous catheter/tube holder.

Other devices from Argentum Medical, LLC

See all devices from Argentum Medical, LLC →

Properties

  • Supplied sterile
  • Single use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)