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B Medical Systems

FDA UDI

Class II (US FDA UDI)

by B Medical Systems SARL

Identity

Trade Name
B Medical Systems FDA UDI
Generic Name
Rapid-contact laboratory freezer FDA UDI
Device Name
Plasma contact shock freezer FDA UDI
Model / Reference
MBF21W FDA UDI
Description
Plasma contact shock freezer FDA UDI

Identifiers

Catalog Number
991.8065.** FDA UDI
Primary DI / UDI-DI
05450104533716 FDA UDI
FDA Product Code
KSE FDA UDI
GMDN Term
Rapid-contact laboratory freezer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9700 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Rapid-contact laboratory freezer

B Medical Systems by B Medical Systems SARL — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rapid-contact laboratory freezer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8cb83852-bc1d-4569-8df8-e56701bc6e7a 35 fields · synced Jun 8, 2026