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Microline 102-137D

by Microline Surgical, Inc.

Microline 102-137D is a Class II device made by Microline Surgical, Inc., listed in FDA GUDID since 13 Nov 2017 (UDI-DI 00811099011408), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00811099011408 UDI-DI Date13 Nov 2017ListedStatusListed GUDID: not in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Microline
Generic name
Electrosurgical handpiece, single-use
Model / Ref / Catalog
102-137D
Primary DI / UDI-DI
00811099011408
FDA product code
GEI
GMDN term
Electrosurgical handpiece, single-use
Device class
Class II
Regulation number
878.4400
GUDID distribution status
Not in Commercial Distribution

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  • ReNew 3411

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See all devices from Microline Surgical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)