Aimsco

GUDID DHT16222

DELTA HI TECH INC

Hypodermic needle, single-use

• Primary Device ID: DHT16222
• NIH Device Record Key: eabff55d-e8ca-4c0c-9c88-6eded65c59ae
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aimsco
• Version Model Number: 622
• Company DUNS: 008597056
• Company Name: DELTA HI TECH INC
• Device Count: 100
• 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: true
• 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
HIBCC	DHT16220 [Unit of Use]
HIBCC	DHT16222 [Primary]

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen

Sterilization

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

[DHT16222]

Ethylene Oxide

[DHT16222]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-10-23
• Device Publish Date: 2017-01-06

On-Brand Devices [Aimsco]

• DHT17442: 744
• DHT17422: 742
• DHT17402: 740
• DHT17222: 722
• DHT16202: 620
• DHT16182: 618
• DHT15292: 529
• DHT15282: 528
• DHT15272: 527
• DHT15262: 526
• DHT15032: 503
• DHT15022: 502
• DHT16322: 632
• DHT16312: 631
• DHT16302: 630
• DHT16222: 622
• DHT16330: Aimsco 32G 5/32 in Pen Needle
• DHT16260: Aimsco 29g 5/16" (8mm) Safety Pen Needle
• DHT16250: Aimsco 29g 3/16" (5mm) Safety Pen Needle