MICROLAN 100 GA553

GUDID 04038653201891

microLAN 100

Aesculap AG

Surgical power tool system handpiece, rotary, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic Bone/joint surgical power tool motorized handpiece/set, pneumatic

• Primary Device ID: 04038653201891
• NIH Device Record Key: d04cf4da-a168-4ec7-abd9-8939402d857b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MICROLAN 100
• Version Model Number: GA553
• Catalog Number: GA553
• Company DUNS: 315018218
• Company Name: Aesculap AG
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04038653201891 [Primary]

FDA Product Code

• GET: MOTOR, SURGICAL INSTRUMENT, PNEUMATIC POWERED

Sterilization

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

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

[04038653201891]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-05-01
• Device Publish Date: 2020-04-23

Devices Manufactured by Aesculap AG

• 04038653180462 - AESCULAP: 2024-04-16 Micro Larynx Scissors, curved to right, working length: 9 3/4", (250 mm), vertical cutting, sharp/sharp, with tubular shaft, rin
• 04038653154838 - AESCULAP: 2024-04-15 SCHUMACHER Biopsy Forceps, straight, 9 1/2", (240 mm)
• 04038653154845 - AESCULAP: 2024-04-15 SCHUMACHER Biopsy Forceps, straight, 9 1/2", (240 mm)
• 04038653154852 - AESCULAP: 2024-04-15 BERGER Biopsy Forceps, straight, 8 1/4", (210 mm)
• 04038653154869 - AESCULAP: 2024-04-15 EPPENDORF Biopsy Forceps, straight, 8", (200 mm)
• 04038653180400 - AESCULAP: 2024-04-15 Micro Laryngeal Ear Forceps, straight, 9 3/4", (250 mm), diam. 2 mm, cup-shaped
• 04038653180417 - AESCULAP: 2024-04-15 Micro Laryngeal Ear Forceps, curved to left, 9 3/4", (250 mm), diam. 2 mm, cup-shaped
• 04046964451812 - VEGA System® PS: 2024-04-08 ALL POLY TIBIA VEGA PS T0 10MM