Scissors 393 100 200

by SOPRO-COMEG GmbH

Scissors 393 100 200 is a Class II device made by SOPRO-COMEG GmbH, listed in FDA GUDID since 12 Sep 2016 (UDI-DI 04059082015941), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04059082015941 UDI-DI	Date12 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 04059082015941

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Scissors
Generic name: Flexible endoscopic scissors, reusable
Model / reference: 393 100 200

Primary DI / UDI-DI: 04059082015941
FDA product code: HRX
GMDN term: Flexible endoscopic scissors, reusable

Device class: Class II
Regulation number: 888.1100
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under Flexible endoscopic scissors, reusable.

Other devices from SOPRO-COMEG GmbH

Bronchoscope 164 055 000BC001

Class II
Grasping forceps 393 910 272

Class II
Arthroscopy sheath 191 240 933BC

Class II
Urology syringe 195 090 200

Class II

See all devices from SOPRO-COMEG GmbH →

Properties

Sterilise before use
Lot / batch number
Manufacturing date

Other properties (12, all answered No)