← Back to catalogue

Reusable Tips Vet Sanalon S

FDA UDI

Class I (US FDA UDI)

by Heine Optotechnik GmbH & Co. KG

Identity

Trade Name
REUSABLE TIPS VET SANALON S FDA UDI
Generic Name
Ear speculum, reusable FDA UDI
Model / Reference
61 mm FDA UDI

Identifiers

Catalog Number
G-000.21.210 FDA UDI
Primary DI / UDI-DI
04053755131280 FDA UDI
FDA Product Code
ERA FDA UDI
GMDN Term
Ear speculum, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4770 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ear speculum, reusable

Reusable Tips Vet Sanalon S by Heine Optotechnik GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ear speculum, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d7b8ab41-0d3f-42f9-befa-10247c5626dc 34 fields · synced Jun 1, 2026