Precision

GUDID 00840050515648

AMERICAN SCREENING, L.L.C.

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• Primary Device ID: 00840050515648
• NIH Device Record Key: 665faeb8-31e8-4f2e-857f-6bfaeece77bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Precision
• Version Model Number: PRES-SAL-164A
• Company DUNS: 169065054
• Company Name: AMERICAN SCREENING, L.L.C.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840050515648 [Primary]

FDA Product Code

• PTG: Test, Methadone, Over The Counter

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-11-21
• Device Publish Date: 2022-11-11

On-Brand Devices [Precision]

• 00840050515709: PRES-SAL-3114A
• 00840050515693: PRES-SAL-3114A
• 00840050515686: PRES-SAL-254
• 00840050515679: PRES-SAL-254
• 00840050515662: PRES-SAL-17104
• 00840050515655: PRES-SAL-17104
• 00840050515648: PRES-SAL-164A
• 00840050515631: PRES-SAL-164A
• 00840050515624: PRES-SAL-164
• 00840050515617: PRES-SAL-164
• 00840050514405: PRENQ-COT-S23
• 00840050514399: PRENQ-COT-S23
• 00840050514382: PREIM-DOA1285N
• 00840050514375: PREIM-DOA1285N
• 00840050514368: PREIM-DOA1284N
• 00840050514351: PREIM-DOA1284N
• 00840050514344: PREIM-DOA1244N
• 00840050514337: PREIM-DOA1244N
• 00840050514320: PREFL-DUD-364N
• 00840050514313: PREFL-DUD-364N
• 00840050514306: PREFLCUP20124N
• 00840050514290: PREFLCUP20124N