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Endocavity Biopsy Starter Kit

FDA UDI

by Protek Medical Products, Inc.

Identity

Trade Name
Endocavity Biopsy Starter Kit FDA UDI
Generic Name
Body-orifice ultrasound imaging transducer cover, basic, non-sterile FDA UDI
Device Name
Stainless Steel Endocavity Biopsy Starter Kit for Alpinion VE3-10H Ultrasound Transducers FDA UDI
Model / Reference
7187 FDA UDI
Description
Stainless Steel Endocavity Biopsy Starter Kit for Alpinion VE3-10H Ultrasound Transducers FDA UDI

Identifiers

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

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Needle guide, reusableBody-orifice ultrasound imaging transducer cover, basicBody-orifice ultrasound imaging transducer cover, basic, non-sterile

Endocavity Biopsy Starter Kit by Protek Medical Products, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Body-orifice ultrasound imaging transducer cover, basic, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Protek Medical Products, Inc.

Sources (1)

  • FDA UDI 893c2884-e263-40fc-bddf-76397908cc37 33 fields · synced May 30, 2026