Identity
- Trade Name
- De Soutter Medical FDA UDI
- Generic Name
- Surgical saw blade, reciprocating, single-use FDA UDI
- Device Name
- RECIP. BLADE - HALL STANDARD (5052-259) 9.4 x 54.5 x 1.00mm FDA UDI
- Model / Reference
- S22-059 FDA UDI
- Description
- RECIP. BLADE - HALL STANDARD (5052-259) 9.4 x 54.5 x 1.00mm FDA UDI
Identifiers
- Catalog Number
- S22-059 FDA UDI
- Primary DI / UDI-DI
- 05051471023567 FDA UDI
- FDA Product Code
- GEY FDA UDI
- GMDN Term
- Surgical saw blade, reciprocating, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Surgical saw blade, reciprocating, single-use
De Soutter Medical by De Soutter Medical, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical saw blade, reciprocating, single-use.
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- IMEDICOM SAW BLADE — IMEDICOM CO., LTD. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- De Soutter Medical, Ltd.
Sources (1)
- FDA UDI 5f5c11df-d884-4e9f-a780-2c122e8e2728 34 fields · synced May 30, 2026