Primary Device ID | 00810607000361 |
NIH Device Record Key | 202de3f9-ef92-4fa5-ae03-37edd0450380 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cranitomy Kit Disposable Low Speed |
Version Model Number | 400-221 |
Catalog Number | 400-221 |
Company DUNS | 612611459 |
Company Name | ACRA-CUT INC |
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 | true |
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 |
00810607000378 | Cranitomy Kit Consisting of Qty 1 - DI810607000095 Cranial Perforator Catalog# 200-283, QTY 1 - |
00810607000361 | Cranitomy Kit Consisting of Qty 1 - D810607000125 Cranial Perforator Catalog# 210-221, QTY 1 - D |
00810607000354 | Cranitomy Kit Consisting of Qty 1 - D810607000101 Cranial Perforator Catalog# 200-331, QTY 1 - D |
00810607000347 | Cranitomy Kit Consisting of Qty 1 - D810607000101 Cranial Perforator Catalog# 200-331, QTY 1 - D |
00810607000330 | Cranitomy Kit Consisting of Qty 1 - D810607000057 Cranial Perforator Catalog# 200-253, QTY 1 - D |
00810607000323 | Cranitomy Kit Consisting of Qty 1 - D810607000057 Cranial Perforator Catalog# 200-253, QTY 1 - D |
00810607000316 | Cranitomy Kit Consisting of Qty 1 - DI810607000071 Cranial Perforator Catalog# 200-271, QTY 1 - |
00810607000309 | Cranitomy Kit Consisting of Qty 1 - DI 810607000019 Cranial Perforator Catalog# 200-241, QTY 1 - |