EXTRACTOR, SPLINTER REMOVER

GUDID 00860009716117

Jhk, Inc.

Screw extractor, single-use

• Primary Device ID: 00860009716117
• NIH Device Record Key: 48b788b5-683c-4b99-9a2f-d90574133e53
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EXTRACTOR, SPLINTER REMOVER
• Version Model Number: 1524
• Company DUNS: 867236309
• Company Name: Jhk, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860009716117 [Primary]

FDA Product Code

• HWB: EXTRACTOR

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-07
• Device Publish Date: 2023-07-28

Devices Manufactured by Jhk, Inc.

• 00860009716179 - ELASTIC BANDAGE: 2023-08-07
• 00860009716117 - EXTRACTOR, SPLINTER REMOVER: 2023-08-07
• 00860009716117 - EXTRACTOR, SPLINTER REMOVER: 2023-08-07
• 00860009716155 - SPRAY / PUMP: 2023-08-07
• 00860009716131 - SCALPEL, ONE-PIECE: 2023-08-07
• 00860009716148 - GAUZE / SPONGE, NONRESORBABLE FOR EXTERNAL USE: 2023-08-07
• 00860009716162 - PACK, HOT OR COLD, DISPOSABLE: 2023-08-07
• 00860009716193 - TAPE AND BANDAGE, ADHESIVE: 2023-08-07