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Vertebroplasty Needle 49632

by Adria SRL

Vertebroplasty Needle 49632 is a Class I device made by Adria SRL, listed in FDA GUDID since 7 Apr 2025 (UDI-DI 08053175016125), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08053175016125 UDI-DI Date7 Apr 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Vertebroplasty Needle
Generic name
Vertebral bone biopsy procedure kit, single-use
Model / reference
49632
Primary DI / UDI-DI
08053175016125
FDA product code
OCJ
GMDN term
Vertebral bone biopsy procedure kit, single-use
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Related devices

Category: Vertebral bone biopsy procedure kit, single-use

Other devices from Adria SRL

See all devices from Adria SRL →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)