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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
Haemodialysis system chlorine monitor FDA UDI
Device Name
FORCEPS SERRATED WITH LOCK, 13CM FDA UDI
Model / Reference
BD-270 FDA UDI
Description
FORCEPS SERRATED WITH LOCK, 13CM FDA UDI

Identifiers

Catalog Number
BD-270 FDA UDI
Primary DI / UDI-DI
04251725222642 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Haemodialysis system chlorine monitor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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: Haemodialysis system chlorine monitor

BMT Medizintechnik GmbH by BMT Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis system chlorine monitor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
BMT Medizintechnik GmbH

Sources (1)

  • FDA UDI f5a794c9-3bd3-4a4f-8389-565fb04da6b8 35 fields · synced May 30, 2026