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Bifurcated Vaccinating Needles

FDA UDI

by Roechling Medical Lancaster, LLC

Identity

Trade Name
Bifurcated Vaccinating Needles FDA UDI
Generic Name
Allergy testing lancet FDA UDI
Device Name
Bifurcated Vaccinating Needles FDA UDI
Model / Reference
PB-01000-000-00 FDA UDI
Description
Bifurcated Vaccinating Needles FDA UDI

Identifiers

Catalog Number
PB-01000-000-00 FDA UDI
Primary DI / UDI-DI
10868652000222 FDA UDI
510(k) Number
K012515 FDA UDI
FDA Product Code
LDH FDA UDI
GMDN Term
Allergy testing lancet FDA UDI

Classification

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

No

FDA UDI

Category: Allergy testing lancet

Bifurcated Vaccinating Needles by Roechling Medical Lancaster, LLC — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Allergy testing lancet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Roechling Medical Lancaster, LLC

Sources (1)

  • FDA UDI 3f02e5d8-6d2a-447c-bc58-5430125b66ac 36 fields · synced Jun 9, 2026