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GreenEgg EP1000-30

by Endoglow, LLC

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860001161618 UDI-DI Date7 Jul 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
GreenEgg
Generic Name
Colonic bougie
Model / Ref / Catalog
EP1000-30
Primary DI / UDI-DI
00860001161618
FDA Product Code
EXX
GMDN Term
Colonic bougie
Device Class
Class I
Regulation Number
876.4730
GUDID distribution status
In Commercial Distribution
Size
Length — 12.5 Inch
Outer Diameter — 30 Millimeter

Related devices

Category: Colonic bougie

Similar devices

Also classified as Colonic bougie.

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No