← Back to catalogue

Black & Black Surgical

FDA UDI

Class II (US FDA UDI)

by Black & Black Surgical, Inc.

Identity

Trade Name
Black & Black Surgical FDA UDI
Generic Name
Cystometer probe, ultrasonic FDA UDI
Device Name
ENDOPLASTIC SCOPE;9''(23.0CM), 30 DEGREE, 5MM DIAMETER FDA UDI
Model / Reference
B65925 FDA UDI
Description
ENDOPLASTIC SCOPE;9''(23.0CM), 30 DEGREE, 5MM DIAMETER FDA UDI

Identifiers

Catalog Number
B65925 FDA UDI
Primary DI / UDI-DI
00840329829322 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Cystometer probe, ultrasonic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Cystometer probe, ultrasonic

Black & Black Surgical by Black & Black Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a14168e0-a441-4d22-8753-7269869e1a17 35 fields · synced May 30, 2026