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Sp

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
SP FDA UDI
Generic Name
Manual scalpel blade, reusable FDA UDI
Device Name
Surgical Blade; Stainless Steel; Size 12 FDA UDI
Model / Reference
D2863-12 FDA UDI
Description
Surgical Blade; Stainless Steel; Size 12 FDA UDI

Identifiers

Catalog Number
D2863-12 FDA UDI
Primary DI / UDI-DI
20630140057479 FDA UDI
FDA Product Code
EMF FDA UDI
GMDN Term
Manual scalpel blade, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

Category: Manual scalpel blade, reusable

Sp by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual scalpel blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI addcde83-2021-414d-8c6e-6f0c4402bb2a 34 fields · synced Jun 6, 2026