← Back to catalogue

Reprocessed Sagittal Blade, 19mm x 90mm x 1.37mm

FDA UDI

Class I (US FDA UDI)

by Suretek Medical

Identity

Trade Name
Reprocessed Sagittal Blade, 19mm x 90mm x 1.37mm FDA UDI
Generic Name
Surgical power tool system handpiece, sawing, line-powered FDA UDI
Model / Reference
S89-6657 FDA UDI

Identifiers

Primary DI / UDI-DI
B390S8966571 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Surgical power tool system handpiece, sawing, line-powered 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 power tool system handpiece, sawing, line-powered

Reprocessed Sagittal Blade, 19mm x 90mm x 1.37mm by Suretek Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool system handpiece, sawing, line-powered.

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
Suretek Medical

Sources (1)

  • FDA UDI 62f714ff-c970-4fb5-839d-4787b43dbf79 32 fields · synced Jun 8, 2026