FDA.reportPublic FDA data

Biopor® AB

Primary DI
E23928216M1
Brand
Biopor® AB
Company
Dreve Otoplastik GmbH
Model
28216M
Catalog number
28216M
Device description
No.
Published
2024-05-08
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information

Contact Domains#

Product Codes#

Code, Name table
CodeName
ESDHearing Aid, Air-Conduction, Prescription

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
ESDHearing Aid, Air-Conduction, PrescriptionEar, Nose, Throat1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
E23928216M1PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Earmould, custom-madeA custom-made device designed to fit in an individual ear, made from an impression of that ear, and through which the acoustic output from a hearing aid is conveyed to the eardrum, or in which transducer components of a hearing aid are aligned. It is made of synthetic polymer materials. This is a reusable device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Storage Environment Temperature18 Degrees Celsius28 Degrees Celsius

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+49230388070otoplastik@dreve.de

Regulatory Flags#

DUNS number
315808340
Device count
1
Premarket exempt
true
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
E239831001FotoTec® Repair83100831002026-10-14
E239284131Biopor® AB28413284132022-08-18
E23928413M1Biopor® AB28413M28413M2022-08-18
E239284331Biopor® AB28433284332022-08-18
E23928433M1Biopor® AB28433M28433M2022-08-18
E239284431Biopor® AB28443284432022-08-18
E23928443M1Biopor® AB28443M28443M2022-08-18
E23971001FotoTec® SL.A710071002022-08-12
E2397100ST1FotoTec® SL.A7100ST7100ST2022-08-12
E23972001FotoTec® SL.A720072002022-08-12
E239032101Libby Horn03210032102022-08-12
E23903211Libby Horn032103212022-08-12
E239031501Libby Horn03150031502022-08-12
E23905651Otoferm® Creme056505652024-06-25
E239904001FotoTec® DLP.C90400904002026-01-30
E239905001FotoTec® DLP.C90500905002026-01-30
E239361001FotoTec® DLP.B36100361002022-09-15
E239906001FotoTec® DLP.C90600906002026-01-15
E2390871SK 87 Silicone glue0870872022-08-12
E239903001FotoTec® DLP.C90300903002025-07-09

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
E239831001FotoTec® RepairDreve Otoplastik GmbHESD2026-10-14
05708296382927BeltoneGn Hearing A/SESD2026-02-10
05708296382934BeltoneGn Hearing A/SESD2026-02-10
05708296382941BeltoneGn Hearing A/SESD2026-02-10
05708296383061BeltoneGn Hearing A/SESD2026-02-10
05708296383078BeltoneGn Hearing A/SESD2026-02-10
05708296383085BeltoneGn Hearing A/SESD2026-02-10
05708296383207BeltoneGn Hearing A/SESD2026-02-10
05708296383214BeltoneGn Hearing A/SESD2026-02-10
05708296383221BeltoneGn Hearing A/SESD2026-02-10
05708296383344BeltoneGn Hearing A/SESD2026-02-10
05708296383351BeltoneGn Hearing A/SESD2026-02-10
05708296383368BeltoneGn Hearing A/SESD2026-02-10
05708296383481GN ReSoundGn Hearing A/SESD2026-02-10
05708296383498GN ReSoundGn Hearing A/SESD2026-02-10
05708296383504GN ReSoundGn Hearing A/SESD2026-02-10
05708296383627GN ReSoundGn Hearing A/SESD2026-02-10
05708296383634GN ReSoundGn Hearing A/SESD2026-02-10
05708296383641GN ReSoundGn Hearing A/SESD2026-02-10
05708296383764GN ReSoundGn Hearing A/SESD2026-02-10
05708296383771GN ReSoundGn Hearing A/SESD2026-02-10
05708296383788GN ReSoundGn Hearing A/SESD2026-02-10
05708296383900GN ReSoundGn Hearing A/SESD2026-02-10
05708296383917GN ReSoundGn Hearing A/SESD2026-02-10
05708296383924GN ReSoundGn Hearing A/SESD2026-02-10
05708296385300GN ReSoundGn Hearing A/SESD2026-02-10
05708296385317GN ReSoundGn Hearing A/SESD2026-02-10
05708296385324GN ReSoundGn Hearing A/SESD2026-02-10
05708296411313BeltoneGn Hearing A/SESD2026-02-10
05708296411320BeltoneGn Hearing A/SESD2026-02-10