Primary Device ID | 00810607000125 |
NIH Device Record Key | 2b64c87c-8247-4bbe-b9e8-784712fcbfd8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Disposable Cranial Perforator |
Version Model Number | 210-221 14/11 mm |
Catalog Number | 210-221 CDM |
Company DUNS | 612611459 |
Company Name | ACRA-CUT 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 | false |
OTC Over-The-Counter | false |
Phone | 9782632210 |
info@acracut.com | |
Phone | 9782632210 |
info@acracut.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810607000125 [Primary] |
HBF | Drills, Burrs, Trephines & Accessories (Compound, Powered) |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00810607000125]
Radiation Sterilization
[00810607000125]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-05-01 |
00810607000125 | Cranial Perforator |
00810607000118 | Cranial Perforator |
00810607000101 | Cranial Perforator |
00810607000095 | Cranial Perforator |
00810607000088 | Cranial Perforator |
00810607000071 | Cranial Perforator |
00810607000064 | Cranial Perforator |
00810607000057 | Cranial Perforator |
00810607000040 | Cranial Perforator |
00810607000033 | Cranial Perforator |
00810607000026 | Cranial Perforator |
00810607000019 | Cranial Perforator |