Integra®

Primary DI
30381780431910
Brand
Integra®
Company
INTEGRA PAIN MANAGEMENT
Model
INS7250
Catalog number
INS7250
Device description
Integra® Cranial Access Kit
Published
2017-11-03
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Related Records

Contact Domains

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
30381780431910PackageGS15In Commercial Distribution
10381780263920PreviousGS10
10381780431916PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalized
3038178043191030381780431910
1038178026392010381780263920
1038178043191610381780431916

GMDN Terms

TermDefinition
Manual cranial rotary handpiece, single-useA manually-powered, hand-held, surgical device intended to be used to remove circular sections of the skull vault (calvarium) to provide access to the interior for diagnosis (e.g., the insertion of a neuroscope), or treatments [e.g., to alleviate intracranial pressure (ICP)], or for the removal of a bone flap for brain surgery. It is typically a drill brace or a housing containing bevelled and/or straight teethed gears rotated via a side handle, and a Jacobs chuck or gripping collet to attach an exchangeable rotating endpiece (e.g., a cranial drill, bur, trephine or perforator). This is a single-use device.

Storage And Handling

TypeLowHighCondition
Special Storage Condition, Specify00Do Not Use If Package Is Damaged
Storage Environment Temperature20 Degrees Celsius25 Degrees Celsius
Storage Environment Temperature68 Degrees Fahrenheit77 Degrees Fahrenheit

Sterilization Methods

Method

Contacts

PhoneEmail
+1(800)654-2873custsvcnj@integralife.com

Regulatory Flags

DUNS number
030370299
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
true
Combination product
true
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company

Primary DIBrandModelCatalogPublished
30381780263917Integra®INS70402016-09-16
30381780263924Integra®INS72502016-09-16
30381780263931Integra®INS72602016-09-16
30381780263948Integra®INS72702016-09-16
30381780263955Integra®INS72802016-09-16
30381780544382Integra®HITHSP04HITHSP042025-08-20
30381780544399Integra®HITHSP06HITHSP062025-08-20
M610310041Integra310042016-12-29
M610310461Integra310462016-12-29
M610310811Integra310812016-12-29
M610311081Integra311082016-12-29
M610311271Integra311272016-12-29
M610311321Integra311322016-12-29
M610311561Integra311562016-12-29
M610312041Integra312042016-12-29
M610105601Integra®10-5602016-09-30
10381780537304Integra®INS5HNDINS5HND2024-11-19
10381780263890Integra®INS030INS0302024-11-19
10381780537328Integra®SP0075SP00752024-11-19
10381780537335Integra®SP0087SP00872024-11-19