PRINTCRAFT PRESS

FDA Device Registration & Listing · Idaho Falls, ID, US · Registration 3013175547

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013175547
FEI Number
3013175547
Entity Name
PRINTCRAFT PRESS
City/State/Country
Idaho Falls, ID, US
Establishment Address
670 S Colorado Ave, Idaho Falls, ID 83402, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
BioTouch Global / Path-tec (Owner Number: 10024021)
Owner / Operator Contact Address
5700 Old Brim Road, Midland, GA 31820, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Urine Transport Kit Blood Alcohol Collection Kit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OHZ Urine Transport Kit (Excludes Hiv Testing) Pathology Class 1 864.3250 2009-08-20
OFM Phlebotomy Blood Collection Kit Cardiovascular Class 2 870.2750 2009-08-20
OIC Blood Alcohol Kit (Excludes Hiv Testing) Clinical Toxicology Class 2 862.3040 2009-08-20

Official Correspondent

Jennifer Block

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BioTouch Global / Path-tec
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3007871198 Path-Tec Midland, GA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013175547. Last updated year: 2026. Please use registration number 3013175547 when referencing this establishment in official correspondence.
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