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HEPRO.US - Blood Collection set with pre-attached holder 23Gx3/4"x12" Pack

FDA UDI

Class II (US FDA UDI)

by Hepro.us Inc.

Identity

Trade Name
HEPRO.US - Blood Collection set with pre-attached holder 23Gx3/4"x12" Pack FDA UDI
Generic Name
Hypodermic needle, single-use FDA UDI
Device Name
Blood Collection SET with pre-attached holder 23G x 3/4" x 12" PE package 50pcs FDA UDI
Model / Reference
BX - Blood Collection Set FDA UDI
Description
Blood Collection SET with pre-attached holder 23G x 3/4" x 12" PE package 50pcs FDA UDI

Identifiers

Primary DI / UDI-DI
00850578007228 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Hypodermic needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Hypodermic needle, single-use

HEPRO.US - Blood Collection set with pre-attached holder 23Gx3/4"x12" Pack by Hepro.us Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Hypodermic needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hepro.us Inc.

Sources (1)

  • FDA UDI 144803fb-4bbf-4049-9f74-c2ba53db1d49 33 fields · synced May 30, 2026