BAR000385

GUDID 10888551013444

BIOPSY FORCEPS ALLIGATOR CUP PRECISOR EXL (BLUE)

STERILMED, INC.

Flexible endoscopic biopsy forceps, reprocessed

• Primary Device ID: 10888551013444
• NIH Device Record Key: 62556664-7479-4bbd-b9fc-ece1851f6b54
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: BAR000385
• Catalog Number: BAR000385
• Company DUNS: 175899459
• Company Name: STERILMED, INC.
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com
• Phone: +1(888)541-0078
• Email: sterilmedcs@its.jnj.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10888551013444 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K042648

FDA Product Code

• NON: Forceps, biopsy, non-electric, reprocessed

Sterilization

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

[10888551013444]

Ethylene Oxide

[10888551013444]

Ethylene Oxide

[10888551013444]

Ethylene Oxide

[10888551013444]

Ethylene Oxide

[10888551013444]

Ethylene Oxide

[10888551013444]

Ethylene Oxide

[10888551013444]

Ethylene Oxide

[10888551013444]

Ethylene Oxide

[10888551013444]

Ethylene Oxide

[10888551013444]

Ethylene Oxide

[10888551013444]

Ethylene Oxide

[10888551013444]

Ethylene Oxide

[10888551013444]

Ethylene Oxide

[10888551013444]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-14
• Device Publish Date: 2020-09-06

Devices Manufactured by STERILMED, INC.

• 10888551045698 - Reprocessed DECANAV EP Catheter, D Curve: 2024-11-25 Reprocessed DECANAV EP Catheter, D Curve, 7Fr, 115cm, Electrodes: 11, SP:2-8-2mm, Tip Length: 2.4mm, Pin Connector:34
• 10888551045704 - Reprocessed DECANAV EP Catheter, F Curve: 2024-11-25 Reprocessed DECANAV EP Catheter, F Curve, 7Fr, 115cm, Electrodes: 11, SP:2-8-2mm, Tip Length: 2.4mm, Pin Connector:34
• 10888551045179 - NA: 2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, F CURVE
• 10888551045186 - NA: 2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, D CURVE
• 10888551045193 - NA: 2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, F CURVE
• 10888551045209 - NA: 2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, D CURVE
• 10888551010313 - NA: 2021-01-22 KNIFE SET ECTRA II (PACK OF 3)
• 10888551021531 - NA: 2021-01-22 KNIVES (1) HOOK BLADE (1) TRIANGLE BLADE ENDOTRAC BLADE SYSTEM