Skip to content

MirusTM Linear Cutter Reload MLCR60-4.8

by Meril Endo Surgery Private Limited

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 Number08906070909606 UDI-DI Date4 May 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  • Withdrawn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
MirusTM Linear Cutter Reload
Generic Name
Open-surgery manual linear cutting stapler, single-use
Model / Reference
MLCR60-4.8
Primary DI / UDI-DI
08906070909606
510(k) Number
FDA Product Code
GDW
GMDN Term
Open-surgery manual linear cutting stapler, single-use
Device Class
Class II
Regulation Number
878.4750
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Cleared under the same submission (K200320)

Show all (12)

Other devices from Meril Endo Surgery Private Limited

See all devices from Meril Endo Surgery Private Limited →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No