← Back to catalogue

Black & Black Surgical, Inc.

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref B66345Model Instrument tray, reusable

by Black & Black Surgical, Inc.

Identity

Trade Name
BLACK & BLACK SURGICAL, INC. FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
STERILIZATION TRAY FOR LIPOSABER HANDPIECE AND CABLE PLUS CANNULA: 20.4" X 9.5" X 2.75", LID, SILICONE MAT FDA UDI
Model / Reference
B66345 EUDAMEDFDA UDI
Instrument tray, reusable EUDAMED
Description
STERILIZATION TRAY FOR LIPOSABER HANDPIECE AND CABLE PLUS CANNULA: 20.4" X 9.5" X 2.75", LID, SILICONE MAT FDA UDI

Identifiers

Catalog Number
B66345 FDA UDI
Primary DI / UDI-DI
00840329833985 EUDAMEDFDA UDI
Basic UDI-DI
08403298011102J2 EUDAMED
FDA Product Code
FSM FDA UDI
EMDN Code
V0402 CLINICAL USE TRAYS AND BOWLS EUDAMED
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

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: Device sterilization/disinfection container, reusable

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

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI c90c3c6d-6be3-4a4d-81f9-2a16668d0d59 35 fields · synced Jun 18, 2026
  • EUDAMED 8becf7e6-e14d-479a-9220-a3cf2f32b484 61 fields · synced Jun 18, 2026