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Peri-Chair LLC chair adjustable

by Peri-Chair, 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 Number00860014545825 UDI-DI Date15 Oct 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  • Withdrawn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
Peri-Chair LLC
Generic Name
Drug-eluting coronary artery stent, fully-bioabsorbable
Model / Reference
chair adjustable
Primary DI / UDI-DI
00860014545825
FDA Product Code
INN
GMDN Term
Drug-eluting coronary artery stent, fully-bioabsorbable
Device Class
Class I
Regulation Number
890.3100
GUDID distribution status
In Commercial Distribution

Properties

  • Implantable
  • Premarket Exempt

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No