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BH Supplies

FDA UDI

Class II (US FDA UDI)

by Anrel Distribution Llc

Identity

Trade Name
BH Supplies FDA UDI
Generic Name
Autoinjector needle FDA UDI
Model / Reference
SPN324 FDA UDI

Identifiers

Primary DI / UDI-DI
00850053135729 FDA UDI
510(k) Number
K192677 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Autoinjector needle 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Autoinjector needle

BH Supplies by Anrel Distribution Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Autoinjector needle.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 59f07084-27ee-4347-bcbf-b1db89d7458d 33 fields · synced May 30, 2026