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Blood Draw Kit with ACD-A

FDA UDI

Class I (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name
Blood Draw Kit with ACD-A FDA UDI
Generic Name
Non-fixed blood collection needle FDA UDI
Device Name
CER-BD-A ASSEMBLY PACK PN 69011-01M FDA UDI
Model / Reference
CER-BD-A FDA UDI
Description
CER-BD-A ASSEMBLY PACK PN 69011-01M FDA UDI

Identifiers

Primary DI / UDI-DI
00850023741639 FDA UDI
FDA Product Code
KDD FDA UDI
GMDN Term
Non-fixed blood collection needle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-fixed blood collection needle

Blood Draw Kit with ACD-A by Ranfac Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-fixed blood collection needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ranfac Corp.

Sources (1)

  • FDA UDI d4d7afea-3445-4b9d-82c8-437026b795f4 35 fields · synced May 30, 2026