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SmartBand Ligation Kit SLK6

by US Endoscopy

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00724995247355 UDI-DI Date21 Nov 2025ListedStatusListed 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  • Withdrawn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
SmartBand Ligation Kit
Generic Name
Oesophageal endoscopic ligator, single-use
Model / Ref / Catalog
SLK6
Primary DI / UDI-DI
00724995247355
FDA Product Code
FHN, MND
GMDN Term
Oesophageal endoscopic ligator, single-use
Device Class
Class II
Regulation Number
876.4400
GUDID distribution status
In Commercial Distribution
Size
Weight — 0.25 Pound
Height — 14 Inch
Width — 10.875 Inch
Depth — 2 Inch

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Properties

  • Single Use
  • Contains Latex
  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (6)

  • Sterile: No
  • Implantable: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No