Endocavity Biopsy Starter Kit 7187

by Protek Medical Products, Inc.

Endocavity Biopsy Starter Kit 7187 is a device made by Protek Medical Products, Inc., listed in FDA GUDID since 17 Mar 2017 (UDI-DI 00841912104956), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00841912104956 UDI-DI	Date17 Mar 2017Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00841912104956

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Endocavity Biopsy Starter Kit
Generic name: Body-orifice ultrasound imaging transducer cover, basic, non-sterile
Model / reference: 7187

Primary DI / UDI-DI: 00841912104956
GMDN term: Body-orifice ultrasound imaging transducer cover, basic, non-sterile

GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

Other devices from Protek Medical Products, Inc.

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Class II
Sterile Disposable Endocavity Needle Guide Kit 5253

Class II
Biopsy Starter Kit 7257

Not classified
Reusable Multi Angle Biospy Bracket 6158

Class II

See all devices from Protek Medical Products, Inc. →

Properties

Sterilise before use
Prescription use
Convenience kit
Lot / batch number
Expiration date
Manufacturing date

Other properties (9, all answered No)