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Adept Medical

FDA UDI

Class I (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name
ADEPT MEDICAL FDA UDI
Generic Name
Tympanotomy knife, single-use FDA UDI
Device Name
MYRINGOTOMY KNIFE STERILE FDA UDI
Model / Reference
38-1400 FDA UDI
Description
MYRINGOTOMY KNIFE STERILE FDA UDI

Identifiers

Catalog Number
38-1400 FDA UDI
Primary DI / UDI-DI
M6333814000 FDA UDI
FDA Product Code
JYP FDA UDI
GMDN Term
Tympanotomy knife, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tympanotomy knife, single-use

Adept Medical by JEDMED Instrument Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tympanotomy knife, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4de9a390-67b1-4bc3-8c10-555df8b28c51 34 fields · synced May 31, 2026