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Retractor, Spinal, quick-connect Blade medial/lateral 19x40mm prongs

FDA UDI

Class II (US FDA UDI)

by Geister Medizin Technik GmbH

Identity

Trade Name
Retractor, Spinal, quick-connect Blade medial/lateral 19x40mm prongs FDA UDI
Generic Name
Surgical retraction system mounting frame, reusable FDA UDI
Device Name
Retractor, Spinal, quick-connect Blade medial/lateral 19x40mm prongs SpineControl™ Titanium (GREEN) FDA UDI
Model / Reference
29-3625.40 FDA UDI
Description
Retractor, Spinal, quick-connect Blade medial/lateral 19x40mm prongs SpineControl™ Titanium (GREEN) FDA UDI

Identifiers

Catalog Number
29-3625.40 FDA UDI
Primary DI / UDI-DI
04057034101049 FDA UDI
FDA Product Code
GZT FDA UDI
GMDN Term
Surgical retraction system mounting frame, reusable 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical retraction system mounting frame, reusable

Retractor, Spinal, quick-connect Blade medial/lateral 19x40mm prongs by Geister Medizin Technik GmbH — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Surgical retraction system mounting frame, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Geister Medizin Technik GmbH

Sources (1)

  • FDA UDI 04b36fb5-8d59-460d-a00c-f390eeb12d23 35 fields · synced May 30, 2026