← Back to catalogue

Saw Blades

FDA UDI

Class I (US FDA UDI)

by Trimed, INC.

Identity

Trade Name
Saw Blades FDA UDI
Generic Name
Surgical saw blade, sagittal, single-use FDA UDI
Device Name
Saw Blade Oscillating, 9mm, S-type FDA UDI
Model / Reference
OSB-9S FDA UDI
Description
Saw Blade Oscillating, 9mm, S-type FDA UDI

Identifiers

Catalog Number
OSB-9S FDA UDI
Primary DI / UDI-DI
00842188109959 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical saw blade, sagittal, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical saw blade, sagittal, single-use

Saw Blades by Trimed, INC. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical saw blade, sagittal, 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
Trimed, INC.

Sources (1)

  • FDA UDI b3e8c72d-f61d-470c-abe5-2a654ef6e3d4 35 fields · synced May 30, 2026