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Microsafe®

FDA UDI

Class I (US FDA UDI)

by Safe-Tec Clinical Products, Inc.

Identity

Trade Name
MICROSAFE® FDA UDI
Generic Name
Capillary blood collection tube IVD, lithium heparin FDA UDI
Model / Reference
1040-50 FDA UDI

Identifiers

Catalog Number
1040-50 FDA UDI
Primary DI / UDI-DI
05060586450106 FDA UDI
FDA Product Code
GIO FDA UDI
GMDN Term
Capillary blood collection tube IVD, lithium heparin FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.6150 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Capillary blood collection tube IVD, lithium heparin

Microsafe® by Safe-Tec Clinical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Capillary blood collection tube IVD, lithium heparin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Safe-Tec Clinical Products, Inc.

Sources (1)

  • FDA UDI ae6cd718-3309-4f8a-80d0-807c73340262 34 fields · synced May 30, 2026