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enforcement Primary ID: Z-0918-2023

Adult Craniotome Ref: CRANI-A-G1 Intended for cutting and shaping bone including the spine and cranium (UDI Z-0918-2023)

Manufactured by The Anspach Effort, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Adult Craniotome Ref: CRANI-A-G1 Intended for cutting and shaping bone including the spine and cranium - Primary ID Z-0918-2023

Device Regulatory Overview

The Adult Craniotome Ref: CRANI-A-G1 Intended for cutting and shaping bone including the spine and cranium (Model/Catalog Number: Unspecified) is a medical device manufactured by The Anspach Effort, Inc.. This product is indexed under FDA Product Code / Category Classification GTIN: 00845384016410 All lots within international Unique Device Identification (UDI) compliance databases.

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Technical Specifications

Model Number
N/A
Device Name
Adult Craniotome Ref: CRANI-A-G1 Intended for cutting and shaping bone including the spine and cranium
Database Sync Date
2026-08-09 10:06:36

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Adult Craniotome Ref: CRANI-A-G1 Intended for cutting and shaping bone including the spine and cranium?

The registered manufacturer of record for Adult Craniotome Ref: CRANI-A-G1 Intended for cutting and shaping bone including the spine and cranium is The Anspach Effort, Inc..

What is the Primary UDI-DI identifier for Adult Craniotome Ref: CRANI-A-G1 Intended for cutting and shaping bone including the spine and cranium?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z-0918-2023.

What classification code is assigned to this device?

This device is registered under product classification code GTIN: 00845384016410 All lots.

Other Devices by The Anspach Effort, Inc.

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