FDA.report

Hand burr

Primary DI
04250676735522
Brand
Hand burr
Company
Spiggle & Theis Medizintechnik GmbH
Model
10-659-07
Catalog number
10-659-07
Device description
diamond, fine 0.7 mm, 16 cm
Published
2022-09-13
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Related Records

Contact Domains

Product Codes

CodeName
LRCINSTRUMENT, ENT MANUAL SURGICAL

Product Code Classifications

CodeDeviceSpecialtyClass
LRCInstrument, Ent Manual SurgicalEar, Nose, Throat1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
04250676735522PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedEAN-13
04250676735522042506767355224250676735522

GMDN Terms

TermDefinition
Corneal bur manual instrumentA hand-held, ophthalmic surgical instrument that consists of a shaft with fluting or cutting planes of steel, or other hard metal, of various shapes at its distal end, used to excavate corneal tissue (e.g., removal of rust rings) through manual rotation. This is a one-piece instrument with no exchangeable components. This is a reusable device.

Sterilization Methods

Method
Moist Heat or Steam Sterilization

Contacts

PhoneEmail
+492206908165c.winterschladen@spiggle-theis.com

Regulatory Flags

DUNS number
332893028
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
true

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