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Davida Neurosurgery Retractor and Hand Stabilization Systems

FDA UDI

Class II (US FDA UDI)

by Flexbar Machine Corp.

Identity

Trade Name
Davida Neurosurgery Retractor and Hand Stabilization Systems FDA UDI
Generic Name
Neurosurgical retraction system, brain FDA UDI
Device Name
9" Tapered Retractor Blade, 1/16" to 1/4" FDA UDI
Model / Reference
38057 FDA UDI
Description
9" Tapered Retractor Blade, 1/16" to 1/4" FDA UDI

Identifiers

Primary DI / UDI-DI
00842102114762 FDA UDI
FDA Product Code
GZT FDA UDI
GMDN Term
Neurosurgical retraction system, brain FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4800 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Neurosurgical retraction system, brain

Davida Neurosurgery Retractor and Hand Stabilization Systems by Flexbar Machine Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurosurgical retraction system, brain.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Flexbar Machine Corp.

Sources (1)

  • FDA UDI c0afa099-81f1-421d-a158-07906c1b743c 33 fields · synced May 30, 2026