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Shaw Scalpel

FDA UDI

Class II (US FDA UDI)

by C2dx, Inc.

Identity

Trade Name
SHAW SCALPEL FDA UDI
Generic Name
Haemostatic knife FDA UDI
Device Name
MODEL 9050 HANDLE - QTY 1 FDA UDI
Model / Reference
7013-9050 FDA UDI
Description
MODEL 9050 HANDLE - QTY 1 FDA UDI

Identifiers

Primary DI / UDI-DI
10850007350250 FDA UDI
510(k) Number
K183009 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Haemostatic knife FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Haemostatic knife

Shaw Scalpel by C2dx, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemostatic knife.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
C2dx, Inc.

Sources (1)

  • FDA UDI 9da4ba8e-6141-4778-a9ae-35630f3cb82e 35 fields · synced May 31, 2026