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Panniculus Retraction Kit: traxi and ABBy - Large PRS-CK-05LG

by Clinical Innovations, 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 Number00814247021328 UDI-DI Date31 May 2026ListedStatusListed 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  • Withdrawn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
Panniculus Retraction Kit: traxi and ABBy - Large
Generic Name
Panniculus skin-adhesive retractor
Model / Reference
PRS-CK-05LG
Primary DI / UDI-DI
00814247021328
FDA Product Code
CCX, KGX
GMDN Term
Panniculus skin-adhesive retractor
Device Class
Class I
Regulation Number
868.6820, 880.5240
GUDID distribution status
In Commercial Distribution

From the manufacturer

Manufacturer's product page: ABBy™ Postoperative Panniculus Retractor

Other devices from Clinical Innovations, LLC

See all devices from Clinical Innovations, LLC →

Properties

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

Other properties (6)

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