OR Specific

Primary DI
10841027103025
Brand
OR Specific
Company
OR SPECIFIC, INC.
Model
420-NS
Device description
Drape, Standard, For 6' Big Case Back Table Model 429 Series. Case of 10. Non-Sterile.- Each
Published
2025-12-08
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
PUIDrape, Surgical, Exempt

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
PUIDrape, Surgical, ExemptGeneral, Plastic Surgery2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10841027103025PackageGS110In Commercial Distribution
00841027103028PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1084102710302510841027103025
00841027103028008410271030288410271030280841027103028

GMDN Terms#

Term, Definition table
TermDefinition
Patient surgical drape, single-useA noninvasive sheet designed to cover a portion of a patient’s anatomy during a surgical procedure to function as a barrier to cross contamination (e.g., isolate a site of surgical incision, protect non-operative anatomy). It is not designed with specific heat-reflective or laser resistant materials. It is available in a variety of designs (e.g., flat sheet with or without an access hole, leg tube or an adhesive film sheet otherwise known as an incise drape). This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
802587928
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00841027102922OR Specific419-S2025-12-08
00841027102939OR Specific419-HDE-NS2025-12-08
00841027102953OR Specific420-HD-NS2025-12-08
00841027102977OR Specific420-HD-S2025-12-08
00841027102984OR Specific418-HD-S2025-12-08
00841027102991OR Specific420-S2025-12-08
00841027103004OR Specific418-S2025-12-08
00841027103011OR Specific418-HDE-S2025-12-08
00841027103028OR Specific420-NS2025-12-08
00841027103035OR Specific420-HDE-S2025-12-08
00841027103042OR Specific419-HD-NS2025-12-08
10841027102929OR Specific419-S2025-12-08
10841027102936OR Specific419-HDE-NS2025-12-08
00841027102946OR Specific419-HDE-S2025-12-08
10841027102950OR Specific420-HD-NS2025-12-08
10841027102974OR Specific420-HD-S2025-12-08
10841027102981OR Specific418-HD-S2025-12-08
10841027102998OR Specific420-S2025-12-08
10841027103001OR Specific418-S2025-12-08
10841027103018OR Specific418-HDE-S2025-12-08

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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30680651501302HalyardO&M HALYARD, INC.PUI2026-06-08
16931918100876AllesetGRI Medical & Electronic Technology Co., Ltd.PUI2026-06-04
16931918102450AllesetGRI Medical & Electronic Technology Co., Ltd.PUI2026-06-04
16931918104201AllesetGRI Medical & Electronic Technology Co., Ltd.PUI2026-06-04
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16931918179179AllesetGRI Medical & Electronic Technology Co., Ltd.PUI2026-06-04
30680651424465HalyardO&M HALYARD, INC.PUI2026-06-02
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