← Back to catalogue

Surgical Direct

FDA UDI

Class I (US FDA UDI)

by Surgical Direct, Inc.

Identity

Trade Name
Surgical Direct FDA UDI
Generic Name
Manual surgical saw blade, flexible, single-use FDA UDI
Device Name
11 1/2 inch Satterlee Saw, Stainless Steel Ring Handle, Straight Tip, Straight Shaft FDA UDI
Model / Reference
SD914025100 FDA UDI
Description
11 1/2 inch Satterlee Saw, Stainless Steel Ring Handle, Straight Tip, Straight Shaft FDA UDI

Identifiers

Catalog Number
SD914025100 FDA UDI
Primary DI / UDI-DI
B382SD9140251000 FDA UDI
FDA Product Code
EIG FDA UDI
GMDN Term
Manual surgical saw blade, flexible, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

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: Manual surgical saw blade, flexible, single-use

Surgical Direct by Surgical Direct, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual surgical saw blade, flexible, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Surgical Direct, Inc.

Sources (1)

  • FDA UDI f0685701-cfb7-48dd-9df0-6ef54c1a36dd 35 fields · synced Jun 1, 2026