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Spectrum, Inc.

FDA UDI

Class II (US FDA UDI)

by Spectrum Co.

Identity

Trade Name
Spectrum, Inc. FDA UDI
Generic Name
Instrument/equipment drape, single-use, non-sterile FDA UDI
Device Name
Equipment Drape, Tear Tip, 7" X 96", Non-sterile FDA UDI
Model / Reference
982-03568-000 FDA UDI
Description
Equipment Drape, Tear Tip, 7" X 96", Non-sterile FDA UDI

Identifiers

Catalog Number
706931NS FDA UDI
Primary DI / UDI-DI
00850301007662 FDA UDI
510(k) Number
K934630 FDA UDI
FDA Product Code
MMP FDA UDI
GMDN Term
Instrument/equipment drape, single-use, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Instrument/equipment drape, single-use, non-sterile

Spectrum, Inc. by Spectrum Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument/equipment drape, single-use, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spectrum Co.

Sources (1)

  • FDA UDI 54876b79-ed63-4e83-930a-807167f4fe27 36 fields · synced Jun 8, 2026