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BMT Medizintechnik GmbH

FDA UDI

Class I (US FDA UDI)

by BMT Medizintechnik GmbH

Identity

Trade Name
BMT Medizintechnik GmbH FDA UDI
Generic Name
Periotome, reusable FDA UDI
Device Name
PERIOTOM FIG.3, 16 CM FDA UDI
Model / Reference
MC-13 FDA UDI
Description
PERIOTOM FIG.3, 16 CM FDA UDI

Identifiers

Catalog Number
MC-13 FDA UDI
Primary DI / UDI-DI
04251725221775 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Periotome, reusable

BMT Medizintechnik GmbH by BMT Medizintechnik GmbH — 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 b559eace-d5e1-4299-b5f4-959b7e5a9d35 35 fields · synced Jun 6, 2026