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ThunderCell Battery Receptacle and Cable+Lamination kit ER01-W-20+MKEB01

by Bionit Labs SRL

Listed FDA GUDID listing, not in commercial distribution

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 Number08057971590834 UDI-DI Date9 Aug 2024ListedStatusListed GUDID: not 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  • Withdrawn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
ThunderCell Battery Receptacle and Cable+Lamination kit
Generic Name
Myoelectric hand prosthesis
Model / Reference
ER01-W-20+MKEB01
Primary DI / UDI-DI
08057971590834
FDA Product Code
IQZ
GMDN Term
Myoelectric hand prosthesis
Device Class
Class I
Regulation Number
890.3420
GUDID distribution status
Not in Commercial Distribution

Other devices from Bionit Labs SRL

Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No