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Microlet® Next 6020

by Ascensia Diabetes Care Us Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number00301936020217 UDI-DI Date16 Mar 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Microlet® Next
Generic Name
Blood lancing device tip
Model / Ref / Catalog
6020, 90012281
Primary DI / UDI-DI
00301936020217
510(k) Number
FDA Product Code
QRK
GMDN Term
Blood lancing device tip
Device Class
Class II
Regulation Number
878.4850
GUDID distribution status
In Commercial Distribution
Size
Needle Gauge — 28 Gauge

Related devices

Cleared under the same submission (K241810)

Other devices from Ascensia Diabetes Care Us Inc.

See all devices from Ascensia Diabetes Care Us Inc. →

Properties

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

Other properties (8)

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