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Blade lateral depth 50mm black

FDA UDI

Class II (US FDA UDI)

by Geister Medizin Technik GmbH

Identity

Trade Name
Blade lateral depth 50mm black FDA UDI
Generic Name
Surgical retraction system mounting frame, reusable FDA UDI
Device Name
Blade lateral depth 50mm black G BLUE LABEL™ FDA UDI
Model / Reference
UL7191-50 FDA UDI
Description
Blade lateral depth 50mm black G BLUE LABEL™ FDA UDI

Identifiers

Catalog Number
UL7191-50 FDA UDI
Primary DI / UDI-DI
04057034264614 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

Blade lateral depth 50mm black by Geister Medizin Technik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 4c1c47ae-5c8b-4cc4-9819-4f3c2d5fe4c4 35 fields · synced May 30, 2026