Primary Device ID | 04250676743688 |
NIH Device Record Key | 78731900-30c4-4336-82e0-e1879062dc04 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Micro- forceps with plateau |
Version Model Number | 40-809-15 |
Catalog Number | 40-809-15 |
Company DUNS | 332893028 |
Company Name | Spiggle & Theis Medizintechnik GmbH |
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 | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +492206908165 |
c.winterschladen@spiggle-theis.com | |
Phone | +492206908165 |
c.winterschladen@spiggle-theis.com | |
Phone | +492206908165 |
c.winterschladen@spiggle-theis.com | |
Phone | +492206908165 |
c.winterschladen@spiggle-theis.com | |
Phone | +492206908165 |
c.winterschladen@spiggle-theis.com | |
Phone | +492206908165 |
c.winterschladen@spiggle-theis.com | |
Phone | +492206908165 |
c.winterschladen@spiggle-theis.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04250676743688 [Primary] |
KAE | FORCEPS, ENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04250676743688]
Moist Heat or Steam Sterilization
[04250676743688]
Moist Heat or Steam Sterilization
[04250676743688]
Moist Heat or Steam Sterilization
[04250676743688]
Moist Heat or Steam Sterilization
[04250676743688]
Moist Heat or Steam Sterilization
[04250676743688]
Moist Heat or Steam Sterilization
[04250676743688]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-09-23 |
Device Publish Date | 2025-09-15 |
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