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Medipin

by Medipin Limited

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 Number05060631140006 UDI-DI Date25 Mar 2021ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Neurological pain-testing pin
Model / Ref / Catalog
Medipin Pack of 100 Esthesiometers/Sensory Testers, MP-100
Primary DI / UDI-DI
05060631140006
FDA Product Code
GXB
GMDN Term
Neurological pain-testing pin
Device Class
Class I
Regulation Number
882.1500
GUDID distribution status
In Commercial Distribution
Size
Length — 80 Millimeter

Related devices

Category: Neurological pain-testing pin

Similar devices

Also classified as Neurological pain-testing pin.

Other devices from Medipin Limited

Properties

  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No