← Back to catalogue

Brasseler USA

FDA UDI

Class I (US FDA UDI)

by Peter Brasseler Holdings, LLC

Identity

Trade Name
Brasseler USA FDA UDI
Generic Name
Surgical saw blade, sagittal, reprocessed FDA UDI
Device Name
S9816 SHORT SERR SAWBLADE 100P FDA UDI
Model / Reference
5024938U0 FDA UDI
Description
S9816 SHORT SERR SAWBLADE 100P FDA UDI

Identifiers

Primary DI / UDI-DI
00887919737315 FDA UDI
FDA Product Code
EBL FDA UDI
GMDN Term
Surgical saw blade, sagittal, reprocessed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3740 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical saw blade, sagittal, reprocessed

Brasseler USA by Peter Brasseler Holdings, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical saw blade, sagittal, reprocessed.

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
Peter Brasseler Holdings, LLC

Sources (1)

  • FDA UDI 11c0c87c-a1ef-472f-80d0-d7417ab799e7 33 fields · synced Jun 8, 2026