← Back to catalogue

Master-Pin-Control

FDA UDI

Class II (US FDA UDI)

by Hager & Meisinger Gesellschaft mit beschränkter Haftung

Identity

Trade Name
Master-Pin-Control FDA UDI
Generic Name
Craniofacial bone tack, non-bioabsorbable FDA UDI
Device Name
The system Master-Pin-Control consist of Pins and neccessary accessories. The system contains 34 Pins. Pins are used for the fixation of membranes (resorbable membranes nonresorbable membranes) to the bone structure. They have a mini-thread and a hexalobular connection for a screwdriver. Pins are intended for single use only. The Pins consist of titanium alloy Grade 5 and are delivered non sterile. FDA UDI
Model / Reference
BMP00 FDA UDI
Description
The system Master-Pin-Control consist of Pins and neccessary accessories. The system contains 34 Pins. Pins are used for the fixation of membranes (resorbable membranes nonresorbable membranes) to the bone structure. They have a mini-thread and a hexalobular connection for a screwdriver. Pins are intended for single use only. The Pins consist of titanium alloy Grade 5 and are delivered non sterile. FDA UDI

Identifiers

Catalog Number
BMP00 FDA UDI
Primary DI / UDI-DI
E0HM79BMP001 FDA UDI
510(k) Number
K130682 FDA UDI
FDA Product Code
DZL FDA UDI
GMDN Term
Craniofacial bone tack, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4880 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Craniofacial bone tack, non-bioabsorbable

Master-Pin-Control by Hager & Meisinger Gesellschaft mit beschränkter Haftung — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Craniofacial bone tack, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c7eb46c8-ae69-4d81-8b91-704ad80b20b6 36 fields · synced Jun 8, 2026