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Shukla Blade S9BLADE

FDA UDI

Class I (US FDA UDI)

by Shukla Medical

Identity

Trade Name
Shukla Blade S9BLADE FDA UDI
Generic Name
Orthopaedic osteotome handle FDA UDI
Device Name
Handle Assy, Osteotome, Push-to-Connect FDA UDI
Model / Reference
SHN012 FDA UDI
Description
Handle Assy, Osteotome, Push-to-Connect FDA UDI

Identifiers

Primary DI / UDI-DI
B756SHN0120 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic osteotome handle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

No

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: Orthopaedic osteotome handle

Shukla Blade S9BLADE by Shukla Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic osteotome handle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shukla Medical

Sources (1)

  • FDA UDI ece348a3-27eb-4f6f-836a-f91af4c7b777 34 fields · synced May 30, 2026