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Medline

FDA UDI

Class U (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Laparoscopic blunt dissector FDA UDI
Device Name
SCD48 @SONICISION CORDLESS ULTRASONIC D FDA UDI
Model / Reference
SCD48RH FDA UDI
Description
SCD48 @SONICISION CORDLESS ULTRASONIC D FDA UDI

Identifiers

Catalog Number
SCD48RH FDA UDI
Primary DI / UDI-DI
10888277681552 FDA UDI
510(k) Number
K170955 FDA UDI
FDA Product Code
NLQ FDA UDI
GMDN Term
Laparoscopic blunt dissector FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laparoscopic blunt dissector

Medline by Medline Industries, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic blunt dissector.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ae376483-776a-4e4b-a29d-7ce038ff979c 36 fields · synced May 30, 2026