Primary Device ID | 00853437006073 |
NIH Device Record Key | 34c2e952-431a-4ee4-b805-041413f842d7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Perma Facial implant |
Version Model Number | PFI 5060 |
Company DUNS | 010030665 |
Company Name | SURGISIL, LLP |
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 |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com | |
Phone | 972.543.2497 |
mikeal@surgisil.com |
Outer Diameter | 5 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 60 Millimeter |
Outer Diameter | 5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00853437006073 [Primary] |
ODU | Facial Implant |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-08-10 |
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