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Intelliguides Intellifuse

by Mios Marketing, LLC 218 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG2710300260240 UDI-DI Date1 Nov 2022ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Intelliguides
Generic Name
Colonic bougie
Model / Ref / Catalog
Intellifuse, 03-0026-024
Primary DI / UDI-DI
G2710300260240
510(k) Number
FDA Product Code
PBF
GMDN Term
Colonic bougie
Device Class
Class II
Regulation Number
888.3030
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
MRI Safety
MR Unsafe
Size
Length — 26 Millimeter
Depth — 24 Millimeter

Related devices

Category: Colonic bougie

Cleared under the same submission (K220717)

Show all (12)

Similar devices

Also classified as Colonic bougie.

Other devices from Mios Marketing, LLC

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Properties

  • Single Use
  • Prescription Use
  • Serial Number

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No