← Back to catalogue

Exact Medical Manufacturing, Inc.

FDA UDI

Class II (US FDA UDI)

by Exact Medical Manufacturing

Identity

Trade Name
Exact Medical Manufacturing, Inc. FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
C-Sheet Standard 137x81cm- 54"x32" FDA UDI
Model / Reference
DI-5417 FDA UDI
Description
C-Sheet Standard 137x81cm- 54"x32" FDA UDI

Identifiers

Catalog Number
DI-5417 FDA UDI
Primary DI / UDI-DI
00850003355344 FDA UDI
FDA Product Code
KKX FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
Not 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Exact Medical Manufacturing, Inc. by Exact Medical Manufacturing — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 480b6f91-c0c4-4370-a541-ff6295142a82 35 fields · synced May 30, 2026