KMS Blade

FDA UDI

Class I (US FDA UDI)

by Gebr. Brasseler GmbH & Co. KG

Identity

Trade Name: KMS Blade FDA UDI
Generic Name: Surgical saw blade, sagittal, single-use FDA UDI
Device Name: Sawblade sterile for Aesculap® Acculan® 90 x 22 x 1,27 mm FDA UDI
Model / Reference: KMS2213.M81.YJ FDA UDI
Description: Sawblade sterile for Aesculap® Acculan® 90 x 22 x 1,27 mm FDA UDI

Identifiers

Catalog Number: KMS2213.M81. FDA UDI
Primary DI / UDI-DI: 14053613158487 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical saw blade, sagittal, single-use

KMS Blade by Gebr. Brasseler GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Surgical saw blade, sagittal, single-use.

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IMEDICOM SAW BLADE — IMEDICOM CO., LTD. · Class I
IMEDICOM SAW BLADE — IMEDICOM CO., LTD. · Class I
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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Gebr. Brasseler GmbH & Co. KG

Sources (1)

FDA UDI dadcb2fe-21fd-4efa-9b8e-281a37638f8e 34 fields · synced Jun 7, 2026