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GEO Sawblade

FDA UDI

Class I (US FDA UDI)

by Gramercy Extremity Orthopedics, Llc.

Identity

Trade Name
GEO Sawblade FDA UDI
Generic Name
Surgical saw blade, sagittal, single-use FDA UDI
Device Name
Saw Blade, 45x13, Sagittal, Stryker Connection FDA UDI
Model / Reference
29104513 FDA UDI
Description
Saw Blade, 45x13, Sagittal, Stryker Connection FDA UDI

Identifiers

Primary DI / UDI-DI
B471291045130 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical saw blade, sagittal, single-use

GEO Sawblade by Gramercy Extremity Orthopedics, Llc. — 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

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Manufacturer

Sources (1)

  • FDA UDI ee74db88-979b-4b64-a318-c2bfb3b9067e 35 fields · synced Jun 8, 2026