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Minicon B15

FDA UDI

Class I (US FDA UDI)

by Merck Millipore Limited

Identity

Trade Name
Minicon B15 FDA UDI
Generic Name
Laboratory dialyser FDA UDI
Model / Reference
9031 FDA UDI

Identifiers

Primary DI / UDI-DI
04054839076244 FDA UDI
FDA Product Code
JJH FDA UDI
GMDN Term
Laboratory dialyser FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2310 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Laboratory dialyser

Minicon B15 by Merck Millipore Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laboratory dialyser.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 460837b8-46ea-45b2-876b-ae6f52419a0b 32 fields · synced May 30, 2026