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Sample Calibrator

FDA UDI

Class II (US FDA UDI)

by Biosafe S.A.

Identity

Trade Name
Sample Calibrator FDA UDI
Generic Name
Blood centrifugation system containment kit FDA UDI
Model / Reference
Sample Calibrator 0.3 ml FDA UDI

Identifiers

Catalog Number
6075 FDA UDI
Primary DI / UDI-DI
07640125650426 FDA UDI
FDA Product Code
OAO FDA UDI
GMDN Term
Blood centrifugation system containment kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9900 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood centrifugation system containment kit

Sample Calibrator by Biosafe S.A. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood centrifugation system containment kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biosafe S.A.

Sources (1)

  • FDA UDI 77fa05ae-d75a-4968-aaa1-6054b8f5c4eb 34 fields · synced Jun 8, 2026