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Reprocessed Radial Max Sagittal Saw Blade, 19.5 x 41 x 0.38mm

FDA UDI

Class I (US FDA UDI)

by Suretek Medical

Identity

Trade Name
Reprocessed Radial Max Sagittal Saw Blade, 19.5 x 41 x 0.38mm FDA UDI
Generic Name
Surgical saw blade, reciprocating, reprocessed FDA UDI
Model / Reference
KM3-254 FDA UDI

Identifiers

Primary DI / UDI-DI
B390KM32541 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical saw blade, reciprocating, reprocessed 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical saw blade, reciprocating, reprocessed

Reprocessed Radial Max Sagittal Saw Blade, 19.5 x 41 x 0.38mm by Suretek Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical saw blade, reciprocating, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Suretek Medical

Sources (1)

  • FDA UDI 94c9338c-09f0-4948-a439-d483a66fc5c1 32 fields · synced May 31, 2026