GUDID 04715309122129

"Panpac Vaginal Dilators are indicated for women who need vaginal dilation for an examination, a surgical procedure, or for the relief of vaginismus.

PANPAC MEDICAL CORPORATION

Vaginal dilator

• Primary Device ID: 04715309122129
• NIH Device Record Key: 270c0407-ea82-4fcd-a174-5774f0b58967
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: DT-A/L
• Company DUNS: 657528899
• Company Name: PANPAC MEDICAL CORPORATION
• Device Count: 1
• DM Exempt: true
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw
• Phone: +866286472242
• Email: service@panpac.com.tw

Device Identifiers

Device Issuing Agency	Device ID
GS1	04715309122129 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130273

FDA Product Code

• HDX: Dilator, Vaginal

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-10

Devices Manufactured by PANPAC MEDICAL CORPORATION

• 04713025222093 - NA: 2020-05-14 Gellhorn pessary is used to relieve the symptoms of cystocele or rectocele and second or third-degree uterine prolapse.
• 04713025222109 - NA: 2020-05-14 Gellhorn pessary is used to relieve the symptoms of cystocele or rectocele and second or third-degree uterine prolapse.
• 04713025222116 - NA: 2020-05-14 Gellhorn pessary is used to relieve the symptoms of cystocele or rectocele and second or third-degree uterine prolapse.
• 04713025222123 - NA: 2020-05-14 Gellhorn pessary is used to relieve the symptoms of cystocele or rectocele and second or third-degree uterine prolapse.
• 04713025222130 - NA: 2020-05-14 Gellhorn pessary is used to relieve the symptoms of cystocele or rectocele and second or third-degree uterine prolapse.
• 04713025222147 - NA: 2020-05-14 Gellhorn pessary is used to relieve the symptoms of cystocele or rectocele and second or third-degree uterine prolapse.
• 04713025222154 - NA: 2020-05-14 Gellhorn pessary is used to relieve the symptoms of cystocele or rectocele and second or third-degree uterine prolapse.
• 04713025222161 - NA: 2020-05-14 Gellhorn pessary is used to relieve the symptoms of cystocele or rectocele and second or third-degree uterine prolapse.