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Bone Management

FDA UDI

Class I (US FDA UDI)

by Hager & Meisinger Gesellschaft mit beschränkter Haftung

Identity

Trade Name
Bone Management FDA UDI
Generic Name
Periotome, reusable FDA UDI
Device Name
Surgical hand-held instrument FDA UDI
Model / Reference
MI193 FDA UDI
Description
Surgical hand-held instrument FDA UDI

Identifiers

Catalog Number
MI193 FDA UDI
Primary DI / UDI-DI
E0HM39MI1931 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Periotome, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

FDA UDI

Lot / Batch Number

Yes

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: Periotome, reusable

Bone Management by Hager & Meisinger Gesellschaft mit beschränkter Haftung — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Periotome, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b3c8f675-085b-4db4-a2cc-eac7c70814c2 35 fields · synced May 31, 2026