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Mk-800800+20

by Microspecialities, 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 Number10810003223422 UDI-DI Date31 Oct 2019ListedStatusListed 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  • Withdrawn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
Keratome blade, single-use
Model / Ref / Catalog
MK-800800+20
Primary DI / UDI-DI
10810003223422
FDA product code
HNO
GMDN term
Keratome blade, single-use
Device class
Class I
Regulation number
886.4370
GUDID distribution status
In Commercial Distribution
Size
Angle — +20 degree

Related devices

Category: Keratome blade, single-use

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  • 300135

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  • 30020

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  • MK8507

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See all devices from Microspecialities, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date

Other properties (9)

  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No