← Back to catalogue

Endoscopic Seal

FDA UDI

Class II (US FDA UDI)

by Obp Corporation

Identity

Trade Name
ENDOSCOPIC SEAL FDA UDI
Generic Name
Endoscope working-channel seal FDA UDI
Device Name
ENDOSCOPIC SEAL GYN 1 SIZE FITS ALL FDA UDI
Model / Reference
C010013 FDA UDI
Description
ENDOSCOPIC SEAL GYN 1 SIZE FITS ALL FDA UDI

Identifiers

Catalog Number
C010013 FDA UDI
Primary DI / UDI-DI
M648C0100130 FDA UDI
FDA Product Code
ODC FDA UDI
GMDN Term
Endoscope working-channel seal FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscope working-channel seal

Endoscopic Seal by Obp Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope working-channel seal.

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

Manufacturer
Obp Corporation

Sources (1)

  • FDA UDI 136f5dbb-326b-4db9-83ee-a1b88b142444 35 fields · synced May 31, 2026