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K2 Lithium-ion battery IBL200HL-MB

by HULASER, Inc.

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08800079000060 UDI-DI Date29 Jul 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  • Withdrawn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
K2 Lithium-ion battery
Generic Name
Portable/mobile rechargeable battery pack
Model / Reference
IBL200HL-MB
Primary DI / UDI-DI
08800079000060
FDA Product Code
MOQ
GMDN Term
Portable/mobile rechargeable battery pack
Device Class
Class I
Regulation Number
878.4820
GUDID distribution status
In Commercial Distribution

Other devices from HULASER, Inc.

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

  • Sterile: No
  • Single Use: 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