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Rna

FDA UDI

by Rna Medical Division

Identity

Trade Name
RNA FDA UDI
Generic Name
Capillary blood collection tube IVD, electrolyte-balanced heparin FDA UDI
Device Name
Safe Wrap Blood Collection Tubes FDA UDI
Model / Reference
CT 220 FDA UDI
Description
Safe Wrap Blood Collection Tubes FDA UDI

Identifiers

Catalog Number
CT 220 FDA UDI
Primary DI / UDI-DI
00851290002195 FDA UDI
GMDN Term
Capillary blood collection tube IVD, electrolyte-balanced heparin FDA UDI

Classification

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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Capillary blood collection tube IVD, electrolyte-balanced heparin

Rna by Rna Medical Division — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Capillary blood collection tube IVD, electrolyte-balanced heparin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rna Medical Division

Sources (1)

  • FDA UDI 2a6f237a-3a00-4ca8-b9c9-528372e20f4a 34 fields · synced Jun 1, 2026